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Thu Apr 24 17:24:22 2003
Articles found doing a Topical Search in Wos with the following string:
(intersex* or inter-sex* or hermaphrodit* or pseudohermaphrodit*) and (human or m?n or wom?n or child or children or boy or boys or girl or girls or patient or patients)
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11396 1994 INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER 4(4):283-287
AARTSEN EJ; SNETHLAGE RAI; VANGEEL AN; GALLEE MPW
SQUAMOUS-CELL CARCINOMA OF THE VAGINA IN A MALE PSEUDOHERMAPHRODITE WITH 5-ALPHA-REDUCTASE DEFICIENCY
00
22298 1993 COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES 316(4):375-383
ABBAS N; MCELREAVEY K; LECONIAT M; VILAIN E; JAUBERT F; BERGER R; NIHOULFEKETE C; RAPPAPORT R; FELLOUS M
FAMILIAL CASE OF 46,XX MALE AND 46,XX TRUE HERMAPHRODITE ASSOCIATED WITH A PATERNAL-DERIVED SRY-BEARING X-CHROMOSOME
144
31151 1990 HUMAN GENETICS 84(4):356-360
ABBAS NE; TOUBLANC JE; BOUCEKKINE C; TOUBLANC M; AFFARA NA; JOB JC; FELLOUS M
A POSSIBLE COMMON ORIGIN OF Y-NEGATIVE HUMAN XX MALES AND XX TRUE HERMAPHRODITES
4425
416457 1995 CURRENT MEDICINAL CHEMISTRY 2(1):583-597
ABELL AD; HENDERSON BR
STEROIDAL AND NONSTEROIDAL INHIBITORS OF STEROID 5-ALPHA- REDUCTASE
311
52533 1996 BRITISH JOURNAL OF RADIOLOGY 69(820):366-367
Ablett MJ; Masters J; Elliott ST
A rapidly expanding testicular mass due to a ruptured ovarian follicle
00
60843 1999 PEDIATRIC SURGERY INTERNATIONAL 15(7):521-522
Abudaia J; Habib Z; Ahmed S
Dermoid cyst: a rare cause of clitorimegaly
11
7043 1966 ACTA BIOLOGICA ACADEMIAE SCIENTIARUM HUNGARICAE 17(3):311-&
ACS T
ARMSTRONG,CN - INTERSEXUALITY IN VERTEBRATES INCLUDING MAN
00
83791 1999 ENDOCRINE JOURNAL 46(2):285-292
Adachi M; Tachibana K; Asakura Y; Suwa S; Nishimura G
A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with 17 alpha-hydroxylase/17,20- lyase deficiency, but without obvious CYP17 gene mutations
20
90350 1993 PEDIATRIC RADIOLOGY 23(1):55-56
ADAMSBAUM C; ROLLAND Y; JOSSO N; KALIFA G
RADIOLOGICAL FINDINGS IN 3 CASES OF PERSISTENT MULLERIAN DUCT SYNDROME
111
100169 1991 CHRONOBIOLOGIA 18(1):9-19
AGUIAR GFD; DASILVA HP; MARQUES N
PATTERNS OF DAILY ALLOCATION OF SLEEP PERIODS - A CASE-STUDY IN AN AMAZONIAN RIVERINE COMMUNITY
10
111254 1992 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 74(3):667-672
AHLGREN R; YANASE T; SIMPSON ER; WINTER JSD; WATERMAN MR
COMPOUND HETEROZYGOUS MUTATIONS (ARG 239-]STOP, PRO 342-]THR) IN THE CYP17 (P45017-ALPHA) GENE LEAD TO AMBIGUOUS EXTERNAL GENITALIA IN A MALE-PATIENT WITH PARTIAL COMBINED 17-ALPHA- HYDROXYLASE 17,20-LYASE DEFICIENCY
346
125904 2000 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 85(2):658-665
Ahmed SF; Cheng A; Dovey L; Hawkins JR; Martin H; Rowland J; Shimura N; Tait AD; Hughes IA
Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome
316
130866 2000 ANNALS OF BOTANY 86(2):211-221
Ainsworth C
Boys and girls come out to play: The molecular biology dioecious plants
80
143980 2001 JAPANESE JOURNAL OF CANCER RESEARCH 92(9):926-932
Akahira JI; Suzuki T; Ito K; Darnel AD; Moriya T; Sato S; Yaegashi N; Okamura K; Sasano H
Expression of 5 alpha-reductases in human epithelial ovarian cancer: Its correlation with androgen receptor status
10
151315 1993 FEBS LETTERS 317(1-2):39-43
AKASAKA Y; KIKUCHI H; NAGAI T; HIRAOKA N; KATO S; HATA J
A POINT MUTATION FOUND IN THE WT1 GENE IN A SPORADIC WILMS- TUMOR WITHOUT GENITOURINARY ABNORMALITIES IS IDENTICAL WITH THE MOST FREQUENT POINT MUTATION IN DENYS-DRASH SYNDROME
212
160286 1993 ADOLESCENT AND PEDIATRIC GYNECOLOGY 6(2):102-104
AKIN JW; THO SPT; MCDONOUGH PG
RECONSIDERING THE DIFFERENCE BETWEEN MIXED GONADAL-DYSGENESIS AND TRUE HERMAPHRODITISM
21
1711009 2001 JOURNAL OF UROLOGY 166(1):225-230
Akman Y; Liu WH; Li YW; Baskin LS
Penile anatomy under the pubic arch: Reconstructive implications
40
187671 1997 POSTGRADUATE MEDICAL JOURNAL 73(866):802-807
Al-Attia HM
Male pseudohermaphroditism due to 5 alpha-reductase-2 deficiency in an Arab kindred
00
196594 1996 PSYCHONEUROENDOCRINOLOGY 21(8):651-657
AlAttia HM
Gender identity and role in a pedigree of Arabs with intersex due to 5 alpha reductase-2 deficiency
52
207648 1997 JOURNAL OF PEDIATRICS 131(3):386-392
Albers N; Ulrichs C; Gluer S; Sinnecker GHG; Mildenberger H; Brodehl J
Etiologic classification of severe hypospadias: Implications for prognosis and management
265
214772 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(1):2-4
Aleck KA; Argueso L; Stone J; Hackel JG; Erickson RP
True hermaphroditism with partial duplication of chromosome 22 and without SRY
73
225525 1996 ANNALS OF SAUDI MEDICINE 16(1):12-15
AlHerbish AS; AlJurayyan NAM; Bakr AMA; Abdullah MA; AlHusain M; AlRabeah AA; Patel PJ; Jawad A; AlSamarrai AI
Sex reassignment: A challenging problem - Current medical and Islamic guidelines
20
230438 1995 ANNALS OF TROPICAL PAEDIATRICS 15(3):203-207
ALJURAYYAN NAM; PATEL PJ; ALHERBISH AS; ABDULLAH MA; ABOBAKR AM; ALRABEEAH AA; JAWAD AJ; ALSAMMARAI AI
AMBIGUOUS GENITALIA - COMPARATIVE ROLE OF PELVIC ULTRASONOGRAPHY AND GENITOGRAPHY
20
240425 1994 TURKISH JOURNAL OF PEDIATRICS 36(4):303-308
ALKIN T; BUYUKGEBIZ A; BAYKARA A
PSYCHOSOCIAL CONSIDERATIONS IN THE MANAGEMENT OF LATE-DIAGNOSED MALE PSEUDOHERMAPHRODITISM
11
251297 1993 CLINICAL PEDIATRICS 32(6):329-333
ALMAGUER MC; SAENGER P; LINDER BL
PHALLIC GROWTH AFTER HCG - A CLINICAL INDEX OF ANDROGEN RESPONSIVENESS
21
262948 2001 ANNALES DE GENETIQUE 44(3):155-159
Alvarez-Nava F; Soto M; Borjas L; Ortiz R; Rojas A; Martinez S; Revol A; Barrera H; Alvarez Z
Molecular analysis of SRY gene in patients with mixed gonadal dysgenesis
30
271628 1997 GENETIC COUNSELING 8(1):7-12
AlvarezNava F; Gonzalez S; Soto M; Martinez C; Prieto M
Complete Androgen Insensitivity Syndrome: Clinical and anatomopathological findings in 23 patients
31
2831077 2002 JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 15(4):423-430
Ammini AC; Gupta R; Kapoor A; Karak A; Kriplani A; Gupta DK; Kucheria K
Etiology, clinical profile, gender identity and long-term follow up of patients with ambiguous genitalia in India
00
290150 1990 CHIRURGIE PEDIATRIQUE 31(4-5):279-283
AMRANI M; RENOIRTE P
TRUE HERMAPHRODITISM LATELY DIAGNOSED - SURGICAL-MANAGEMENT WITH A 15 YEARS FOLLOW-UP
22
300946 2001 AMERICAN JOURNAL OF BOTANY 88(2):220-233
Anderson GJ; Bernardello G; Stuessy TF; Crawford DJ
Breeding system and pollination of selected plants endemic to Juan Fernandez Islands
70
312560 1996 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 81(3):902-908
Anderson RA; Wallace AM; Wu FCW
Comparison between testosterone enanthate-induced azoospermia and oligozoospermia in a male contraceptive study .3. Higher 5 alpha-reductase activity in oligozoospermic men administered supraphysiological doses of testosterones
361
322201 1991 NATURE 354(6349):159-161
ANDERSSON S; BERMAN DM; JENKINS EP; RUSSELL DW
DELETION OF STEROID 5-ALPHA-REDUCTASE 2-GENE IN MALE PSEUDOHERMAPHRODITISM
378127
331486 1995 JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY 53(1-6):37-39
ANDERSSON S; GEISSLER WM; PATEL S; WU L
THE MOLECULAR-BIOLOGY OF ANDROGENIC 17-BETA-HYDROXYSTEROID DEHYDROGENASES
192
342674 1997 STEROIDS 62(1):143-147
Andersson S; Moghrabi N
Physiology and molecular genetics of 17 beta-hydroxysteroid dehydrogenases
424
358785 1999 BRITISH JOURNAL OF DERMATOLOGY 141(5):840-845
Ando Y; Yamaguchi Y; Hamada K; Yoshikawa K; Itami S
Expression of mRNA for androgen receptor, 5 alpha-reductase and 17 beta-hydroxysteroid dehydrogenase in human dermal papilla cells
81
361116 1981 CLINICAL GENETICS 20(4):289-295
ANNEREN G; FRYKBERG T; GUSTAVSON KH
A BOY WITH TRUE HERMAPHRODITISM AND SEX-CHROMOSOME MOSAICISM AND A FERTILE WOMAN WITH TURNER MOSAICISM IN A FAMILY WITH A TRANSLOCATION 8P-19P
11
375640 1997 JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY 50(1):51-52
Anwar R; Gilbey SG; New JP; Markham AF
Male pseudohermaphroditism resulting from a novel mutation in the human steroid 5 alpha-reductase type 2 gene (SRD5A2)
31
380180 1991 HISTOPATHOLOGY 18(6):541-547
ARMSTRONG GR; BUCKLEY CH; KELSEY AM
GERM-CELL EXPRESSION OF PLACENTAL ALKALINE-PHOSPHATASE IN MALE PSEUDOHERMAPHRODITISM
82
390393 1994 HUMAN GENETICS 93(4):389-393
ARN P; CHEN H; TUCKMULLER CM; MANKINEN C; WACHTEL G; LI SB; SHEN CC; WACHTEL SS
SRVX, A SEX REVERSING LOCUS IN XP21.2-]P22.11
362
401626 1997 FERTILITY AND STERILITY 67(2):394-397
Arnhold IJP; Latronico AC; Batista MC; Carvalho FM; Chrousos GP; Mendonca BB
Ovarian resistance to luteinizing hormone: A novel cause of amenorrhea and infertility
53
4111788 1999 CLINICAL ENDOCRINOLOGY 51(6):701-707
Arnhold IJP; Latronico AC; Batista MC; Izzo CR; Mendonca BB
Clinical features of women with resistance to luteinizing hormone
21
427802 1999 FERTILITY AND STERILITY 71(4):597-601
Arnhold IJP; Latronico AC; Batista MC; Mendonca BB
Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene
63
4311985 2001 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 86(6):2875-2880
Asada Y; Sonoda T; Ojiro M; Kurata S; Sato T; Ezaki T; Takayasu S
5 alpha-Reductase type 2 is constitutively expressed in the dermal papilla and connective tissue sheath of the hair follicle in vivo but not during culture in vitro
20
4441074 2002 JOURNAL OF MOLECULAR MEDICINE-JMM 80(12):782-790
Assumpcao JG; Benedetti CE; Maciel-Guerra AT; Guerra G; Baptista MTM; Scolfaro MR; de Mello MP
Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypes
00
45528 1962 LANCET 2(7245):20-&
ATKINS L; ENGEL E
ABSENCE OF Y CHROMOSOME (XO SEX-CHROMOSOME CONSTITUTION) IN A HUMAN INTERSEX WITH AN EXTRA-ABDOMINAL TESTIS
341
4661143 2003 JOURNAL OF PEDIATRIC SURGERY 38(1):124-129
Auber F; Lortat-Jacob S; Sarnacki S; Jaubert F; Salomon R; Thibaud E; Jeanpierre C; Nihoul-Fekete C
Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes)
00
476514 1996 ACTA ANATOMICA 156(4):241-252
Aumuller G; Eicheler W; Renneberg H; Adermann K; Vilja P; Forssmann WG
Immunocytochemical evidence for differential subcellular localization of 5 alpha-reductase isoenzymes in human tissues
155
480401 1994 JOURNAL OF GYNECOLOGIC SURGERY 10(3):169-172
AYHAN A; KAYA H; TUNCER ZS; KAPUCU R; DURUKAN T; KISNISCI HA
SURGERY FOR CONGENITAL ABSENCE OF THE VAGINA - RESULTS AND COMPLICATIONS OF 108 CONSECUTIVE PATIENTS
00
491214 1992 AMERICAN JOURNAL OF DISEASES OF CHILDREN 146(10):1218-1223
BAILEY WA; ZWINGMAN TA; REZNIK VM; GRISWOLD WR; MENDOZA SA; JONES KL; FREIDENBERG GR
END-STAGE RENAL-DISEASE AND PRIMARY HYPOGONADISM ASSOCIATED WITH A 46,XX KARYOTYPE
114
500268 1992 JOURNAL OF UROLOGY 148(2):680-682
BAILEZ MM; GEARHART JP; MIGEON C; ROCK J
VAGINAL RECONSTRUCTION AFTER INITIAL CONSTRUCTION OF THE EXTERNAL GENITALIA IN GIRLS WITH SALT-WASTING ADRENAL- HYPERPLASIA
121
510582 1996 JOURNAL OF UROLOGY 156(2):854-856
Balaji KC; Caldamone AA; Rabinowitz R; Ortenberg J; Diamond DA
Splenogonadal fusion
80
521276 1992 PEDIATRIC PATHOLOGY 12(1):29-49
BALE PM; HOWARD NJ; WRIGHT JE
MALE PSEUDOHERMAPHRODITISM IN XY CHILDREN WITH FEMALE PHENOTYPE
64
5301020 2001 NETHERLANDS JOURNAL OF ZOOLOGY 51(3):347-360
Baminger H; Haase M
Spermatophore formation in the simultaneously hermaphroditic land snail Arianta arbustorum (Pulmonata : Stylommatophora : Helicidae)
00
54093 1977 JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY 8(12):R18-R18
BARBARINO A; LAFUENTI G; MUSCATELLO P; MATTEUCCI BR; DEMARINIS L
GONADOTROPIN AND PROLACTIN MEASUREMENTS AFTER ESTROGEN ADMINISTRATION TO ADULT PATIENTS WITH MALE PSEUDOHERMAPHRODITISM AND KLINEFELTERS-SYNDROME
00
555662 1997 NATURE GENETICS 17(4):467-470
Barbaux S; Niaudet P; Gubler MC; Grunfeld JP; Jaubert F; Kuttenn F; Fekete CN; SouleyreauTherville N; Thibaud E; Fellous M; McElreavey K
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
14120
560461 1995 ETHOLOGY AND SOCIOBIOLOGY 16(5):395-424
Barber N
The evolutionary psychology of physical attractiveness: Sexual selection and human morphology
610
578808 1999 HUMAN MUTATION 13(2):146-153
Barbosa AS; Hadjiathanasiou CG; Theodoridis C; Papathanasiou A; Tar A; Merksz M; Gyorvari B; Sultan C; Dumas R; Jaubert F; Niaudet P; Moreira CA; Cotinot C; Fellous M
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
185
580767 1998 WATER AIR AND SOIL POLLUTION 103(1-4):173-195
Barcan VS; Kovnatsky EF; Smetannikova MS
Absorption of heavy metals in wild berries and edible mushrooms in an area affected by smelter emissions
80
590540 1996 EMBO JOURNAL 15(17):4477-4484
Barnes TM; Hodgkin J
The tra-3 sex determination gene of Caenorhabditis elegans encodes a member of the calpain regulatory protease family
450
600839 1999 NATURE 401(6751):386-389
Barr MM; Sternberg PW
A polycystic kidney-disease gene homologue required for male mating behaviour in C-elegans
560
613926 2000 JOURNAL OF UROLOGY 164(2):497-501
Barthold JS; Kumasi-Rivers K; Upadhyay J; Shekarriz B; Imperato-McGinley J
Testicular position in the androgen insensitivity syndrome: Implications for the role of androgens in testicular descent
60
6211888 2000 EUROPEAN UROLOGY 37(4):367-380
Bartsch G; Rittmaster RS; Klocker H
Dihydrotestosterone and the concept of 5 alpha-reductase inhibition in human benign prostatic hyperplasia
170
63101131 2002 UROLOGE A 41(5):412-+
Bartsch G; Rittmaster RS; Klocker H
Dihydrotestosterone and the role of 5-alpha-reductase inhibitors in benign prostate hyperplasia
00
64111134 2002 WORLD JOURNAL OF UROLOGY 19(6):413-425
Bartsch G; Rittmaster RS; Klocker H
Dihydrotestosterone and the concept of 5 alpha-reductase inhibition in human benign prostatic hyperplasia
10
650833 1999 JOURNAL OF UROLOGY 162(3):1015-1020
Baskin LS; Erol A; Li YW; Liu WH; Kurzrock E; Cunha GR
Anatomical studies of the human clitoris
144
663128 1984 REVISTA DE INVESTIGACION CLINICA 36(3):231-235
BASSOL S; ULLOAAGUIRRE A; PEREZ AE; MENDEZ JP; PEREZPALACIOS G
5 ALPHA-REDUCTASE AND 17 BETA-OXIDOREDUCTASE STEROID ACTIVITIES IN HUMAN-FIBROBLASTS - STUDY OF PATIENTS WITH DIFFERENT FORMS OF PSEUDOHERMAPHRODITISM
10
672958 2001 CLINICAL GENETICS 59(1):52-57
Batanian JR; Grange DK; Fleming R; Gadre B; Wetzel J
Two unbalanced translocations involving a common 6p25 region in two XY female patients
00
680408 1994 JOURNAL OF REPRODUCTIVE MEDICINE 39(7):541-543
BATZER FR; NELSON JR; CORSON SL; GOCIAL B
LAPAROSCOPIC APPROACH TO DEFINITIVE TREATMENT OF ANDROGEN INSENSITIVITY SYNDROME - A CASE-REPORT
41
6904 1952 ACTA MEDICA SCANDINAVICA 142(3):162-176
BAUER J
PROBLEMS OF HUMAN INTERSEXUALITY - GENETIC AND ENDOCRINE INTERACTION
20
700205 1991 REPRODUCTION FERTILITY AND DEVELOPMENT 3(3):267-276
BEAMER WG; WHITTEN WK
DO HISTOCOMPATIBILITY GENES INFLUENCE SEX-RATIO (PERCENT-MALES)
30
710977 2001 HUMAN MOLECULAR GENETICS 10(9):963-972
Bean CJ; Hunt PA; Millie EA; Hassold TJ
Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone
50
726723 1998 JOURNAL OF CLINICAL INVESTIGATION 102(7):1352-1359
Beau I; Touraine P; Meduri G; Gougeon A; Desroches A; Matuchansky C; Milgrom E; Kuttenn F; Misrahi W
A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor
426
730271 1992 MARINE ECOLOGY-PUBBLICAZIONI DELLA STAZIONE ZOOLOGICA DI NAPOLI I 13(4):363-373
BECERRO MA; TURON X
REPRODUCTIVE-CYCLES OF THE ASCIDIANS MICROCOSMUS-SABATIERI AND HALOCYNTHIA-PAPILLOSA IN THE NORTHWESTERN MEDITERRANEAN
70
7410912 2000 JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION 23(9):566-572
Beck-Peccoz P; Romoli R; Persani L
Mutations of LH and FSH receptors
50
752285 1993 ACTA ENDOCRINOLOGICA 128(2):161-167
BECKMANN MW; WIEACKER P; DERESER MM; FLECKEN U; BRECKWOLDT M
INFLUENCE OF STEROID-HORMONES ON 5-ALPHA-REDUCTASE ACTIVITY IN FEMALE AND MALE GENITAL SKIN FIBROBLASTS IN CULTURE
71
760125 1983 UROLOGY 22(6):604-607
BEHESHTI M; HARDY BE; CHURCHILL BM; DANEMAN D
GENDER ASSIGNMENT IN MALE PSEUDOHERMAPHRODITE CHILDREN
85
770121 1982 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 54(4):698-704
BELGOROSKY A; RIVAROLA MA
SEX HORMONE-BINDING GLOBULIN RESPONSE TO HUMAN CHORIONIC- GONADOTROPIN STIMULATION IN CHILDREN WITH CRYPTORCHIDISM, ANORCHIA, MALE PSEUDO-HERMAPHRODITISM, AND MICRO-PENIS
292
780336 1993 JOURNAL OF UROLOGY 150(2):651-653
BELLINGER MF
SUBTOTAL DEEPITHELIALIZATION AND PARTIAL CONCEALMENT OF THE GLANS CLITORIS - A MODIFICATION TO IMPROVE THE COSMETIC RESULTS OF FEMINIZING GENITOPLASTY
21
793774 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 89(4):218-223
Belville C; Josso N; Picard JY
Persistence of mullerian derivatives in males
213
803913 2000 JOURNAL OF EXPERIMENTAL ZOOLOGY 286(7):745-754
Beolchini F; Rebecchi L; Capanna E; Bertolani R
Female gonad of moles, genus Talpa (Insectivora, Mammalia): Ovary or ovotestis?
00
812769 1999 ACTA PAEDIATRICA 88(11):1229-1232
Berensztein E; Torrado M; Belgorosky A; Rivarola M
Smith-Lemli-Opitz syndrome: in vivo and in vitro study of testicular function in a prepubertal patient with ambiguous genitalia
10
82099 1978 PEDIATRIC RESEARCH 12(10):1029-1029
BERGADA C; COCO R
POSSIBLE EVIDENCE OF Y-CHROMOSOME IN TESTICULAR TISSUE OF PATIENTS WITH TRUE HERMAPHRODITISM AND KARYOTYPE 46,XX
00
83125 1962 ACTA ENDOCRINOLOGICA 40(4):493-&
BERGADA C; WILKINS L; JONES HW; CLEVELAND WW
GONADAL HISTOLOGY IN PATIENTS WITH MALE PSEUDOHERMAPHRODITISM AND ATYPICAL GONADAL DYSGENESIS - RELATION TO THEORIES OF SEX DIFFERENTIATION
897
840284 1992 WIENER TIERARZTLICHE MONATSSCHRIFT 79(7):212-214
BERGER B; GRABHERR H; FISCHERLEITNER F
GENE-FREQUENCIES AND PHENOTYPICAL EXPRESSION OF SOME IMPORTANT HEREDITARY DEFECTS IN PIGS AS A BASIS FOR PRACTICAL PROGENY TESTING
00
851612 1997 BRITISH JOURNAL OF UROLOGY 79(1):122-126
Berkmen F
Persistent Mullerian duct syndrome with or without transverse testicular ectopia and testis tumours
103
863246 1992 HUMAN GENETICS 88(4):411-416
BERKOVITZ GD; FECHNER PY; MARCANTONIO SM; BLAND G; STETTEN G; GOODFELLOW PN; SMITH KD; MIGEON CJ
THE ROLE OF THE SEX-DETERMINING REGION OF THE Y-CHROMOSOME (SRY) IN THE ETIOLOGY OF 46,XX TRUE HERMAPHRODITISM
6733
871239 1992 HORMONE RESEARCH 37(3):103-106
BERTA P; MORIN D; POULAT F; TAVIAUX S; LOBACCARO JM; SULTAN C; DUMAS R
MOLECULAR ANALYSIS OF THE SEX-DETERMINING REGION FROM THE Y- CHROMOSOME IN 2 PATIENTS WITH FRASIER SYNDROME
104
883670 1997 PEDIATRIC RESEARCH 41(2):266-271
Bertelloni S; Federico G; Baroncelli GI; Cavallo L; Corsello G; Liotta A; Rigon F; Saggese G
Biochemical selection of prepubertal patients with androgen insensitivity syndrome by sex hormone-binding globulin response to the human chorionic gonadotropin test
40
890795 1999 ESPRIT (2):193-198
Bessard-Banquy O
The new order of emotions - Observations on the sociology of intersexuality and man-woman interaction
00
901198 1991 KLINICHESKAYA MEDITSINA 69(12):16-21
BEZVERKHAYA TP
ANDROGEN RESISTANCE RELATED TO RECEPTION ABNORMALITIES
00
910347 1993 NEUROLOGY 43(10):2006-2010
BHATIA S; BOOKHEIMER SY; GAILLARD WD; THEODORE WH
MEASUREMENT OF WHOLE TEMPORAL-LOBE AND HIPPOCAMPUS FOR MR VOLUMETRY - NORMATIVE DATA
580
924442 1995 BIOCHEMISTRY 34(11):3663-3669
BHATTACHARYYA AK; CHAVAN AJ; HALEY BE; TAYLOR MF; COLLINS DC
IDENTIFICATION OF THE NADP(H) BINDING-SITE OF RAT-LIVER MICROSOMAL 5-ALPHA-REDUCTASE (ISOZYME-1) - PURIFICATION OF A PHOTOLABELED PEPTIDE CORRESPONDING TO THE ADENINE BINDING DOMAIN
125
937850 1999 STEROIDS 64(3):197-204
Bhattacharyya AK; Wang M; Rajagopalan K; Taylor MF; Hiipakka R; Liao S; Collins DC
Analysis of the steroid binding domain of rat steroid 5 alpha- reductase (isozyme-1) - The steroid D-ring binding domain of 5 alpha-reductase
41
942200 1991 MOLECULAR ENDOCRINOLOGY 5(12):2037-2045
BIASON A; MANTERO F; SCARONI C; SIMPSON ER; WATERMAN MR
DELETION WITHIN THE CYP17-GENE TOGETHER WITH INSERTION OF FOREIGN DNA IS THE CAUSE OF COMBINED COMPLETE 17 ALPHA- HYDROXYLASE/17,20-LYASE DEFICIENCY IN AN ITALIAN PATIENT
203
950860 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(6):1563-1568
Biason-Lauber A; Schoenle EJ
Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency
250
965702 1998 EUROPEAN JOURNAL OF ENDOCRINOLOGY 139(3):330-333
Bilbao JR; Loridan L; Audi L; Gonzalo E; Castano L
A novel missense (R80W) mutation in 17-beta-hydroxysteroid dehydrogenase type 3 gene associated with male pseudohermaphroditism
30
975528 1996 BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 6(13):1517-1522
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