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Results: 1-23 |
Results: 23
MOLECULAR ANALYSIS OF THE Y-CHROMOSOME IN INFERTILE MEN
Authors: QUINTANAMURCI L BARBAUX S SIFFROI JP DELAFONTAINE D ROUBA H KRAUSZ C SOULEYREAUTHERVILLE N JEANDIDIER E PLESSIS G BOURGERON T FELLOUS M MCELREAVEY K FELLOUS M MCELREAVEY K
Citation: L. Quintanamurci et al., MOLECULAR ANALYSIS OF THE Y-CHROMOSOME IN INFERTILE MEN, European journal of human genetics, 6, 1998, pp. 2107-2107
GENETICS AND NEPHROTIC SYNDROMES
Authors: NIAUDET P BROYER M GUBLER MC JEANPIERRE C BARBAUX S ANTIGNAC C
Citation: P. Niaudet et al., GENETICS AND NEPHROTIC SYNDROMES, Archives de pediatrie, 5, 1998, pp. 152-155
HIGH-FREQUENCY OF WELL-DEFINED Y-CHROMOSOME DELETIONS IN IDIOPATHIC SERTOLI CELL-ONLY SYNDROME
Authors: FORESTA C FERLIN A GAROLLA A MORO E PISTORELLO M BARBAUX S ROSSATO M
Citation: C. Foresta et al., HIGH-FREQUENCY OF WELL-DEFINED Y-CHROMOSOME DELETIONS IN IDIOPATHIC SERTOLI CELL-ONLY SYNDROME, Human reproduction, 13(2), 1998, pp. 302-307
STERILITY AND HEREDITARY
Authors: BARBAUX S FELLOUS M
Citation: S. Barbaux et M. Fellous, STERILITY AND HEREDITARY, Contraception fertilite sexualite, 25(3), 1997, pp. 192-193
DONOR SPLICE-SITE MUTATIONS IN WT1 ARE RESPONSIBLE FOR FRASIER-SYNDROME
Authors: BARBAUX S NIAUDET P GUBLER MC GRUNFELD JP JAUBERT F KUTTENN F FEKETE CN SOULEYREAUTHERVILLE N THIBAUD E FELLOUS M MCELREAVEY K
Citation: S. Barbaux et al., DONOR SPLICE-SITE MUTATIONS IN WT1 ARE RESPONSIBLE FOR FRASIER-SYNDROME, Nature genetics, 17(4), 1997, pp. 467-470
GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE (VOL 41, PG 227, 1997)
Authors: SEBOUN E BARBAUX S BOURGERON T NISHI S ALGONIK A EGASHIRA M NIKKAWA N BISHOP C FELLOUS M MCELREAVEY K KASAHARA M
Citation: E. Seboun et al., GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE (VOL 41, PG 227, 1997), Genomics, 45(2), 1997, pp. 477-477
GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE
Authors: SEBOUN E BARBAUX S BOURGERON T NISHI S ALGONIK A EGASHIRA M NIKKAWA N BISHOP C FELLOUS M MCELREAVEY K KASAHARA M
Citation: E. Seboun et al., GENE SEQUENCE, LOCALIZATION, AND EVOLUTIONARY CONSERVATION OF DAZLA, A CANDIDATE MALE-STERILITY GENE, Genomics, 41(2), 1997, pp. 227-235
TRUE HERMAPHRODITISM - CLINICAL ASPECTS AND MOLECULAR STUDIES IN 16 CASES
Authors: DAMIANI D FELLOUS M MCELREAVEY K BARBAUX S BARRETO ESA DICHTCHEKENIAN V SETIAN N
Citation: D. Damiani et al., TRUE HERMAPHRODITISM - CLINICAL ASPECTS AND MOLECULAR STUDIES IN 16 CASES, European journal of endocrinology, 136(2), 1997, pp. 201-204
MUTATIONS AND SEQUENCE VARIANTS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN INDIVIDUALS WITH A 46,XY FEMALE PHENOTYPE
Authors: VEITIA R ION A BARBAUX S JOBLING MA SOULEYREAU N ENNIS K OSTRER H TOSI M MEO T CHIBANI J FELLOUS M MCELREAVEY K
Citation: R. Veitia et al., MUTATIONS AND SEQUENCE VARIANTS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN INDIVIDUALS WITH A 46,XY FEMALE PHENOTYPE, Human genetics, 99(5), 1997, pp. 648-652
HYPERTELORISM AND HYPOSPADIAS ASSOCIATED WITH A DE-NOVO APPARENTLY BALANCED TRANSLOCATION BETWEEN 8Q22.3-23 AND 20P13
Authors: TAR A ION A SOLYOM J GYORVARI B STEPHENSON C BARBAUX S NUNES M FELLOUS M MCELREAVEY K
Citation: A. Tar et al., HYPERTELORISM AND HYPOSPADIAS ASSOCIATED WITH A DE-NOVO APPARENTLY BALANCED TRANSLOCATION BETWEEN 8Q22.3-23 AND 20P13, American journal of medical genetics, 68(2), 1997, pp. 231-235
Y-CHROMOSOME DELETIONS IN IDIOPATHIC SEVERE TESTICULOPATHIES
Authors: FORESTA C FERLIN A GAROLLA A ROSSATO M BARBAUX S DEBORTOLI A
Citation: C. Foresta et al., Y-CHROMOSOME DELETIONS IN IDIOPATHIC SEVERE TESTICULOPATHIES, The Journal of clinical endocrinology and metabolism, 82(4), 1997, pp. 1075-1080
DONOR SPLICE-SITE MUTATIONS IN THE WILMS-TUMOR GENE, WT1 ARE RESPONSIBLE FOR FRAZIER-SYNDROME
Authors: BARBAUX S NIAUDET P GUBLER MC GRUNFELD JP JAUBERT F KUTTENN F FEKETE CN SOULEYREAUTHERVILLE N THIBAUD E FELLOUS M MCELREAVEY K
Citation: S. Barbaux et al., DONOR SPLICE-SITE MUTATIONS IN THE WILMS-TUMOR GENE, WT1 ARE RESPONSIBLE FOR FRAZIER-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1905-1905
GENETICS OF MALE-INFERTILITY
Authors: BOURGERON T BARBAUX S MCELREAVEY K FELLOUS M
Citation: T. Bourgeron et al., GENETICS OF MALE-INFERTILITY, MS. Medecine sciences, 12(11), 1996, pp. 1-8
THE XENOPUS-LAEVIS HOMOLOG OF THE 64-KDA SUBUNIT OF CLEAVAGE STIMULATION FACTOR
Authors: BARBAUX S SEERY LT SCHOENBERG DR SELLAR GC WHITEHEAD AS
Citation: S. Barbaux et al., THE XENOPUS-LAEVIS HOMOLOG OF THE 64-KDA SUBUNIT OF CLEAVAGE STIMULATION FACTOR, Comparative biochemistry and physiology. B. Comparative biochemistry, 114(3), 1996, pp. 313-315
THE ACTIVITY OF THE HIGHLY INDUCIBLE MOUSE PHENYLALANINE-HYDROXYLASE GENE PROMOTER IS DEPENDENT UPON A TISSUE-SPECIFIC, HORMONE-INDUCIBLE ENHANCER
Authors: FAUST DM CATHERIN AM BARBAUX S BELKADI L IMAIZUMISCHERRER T WEISS MC
Citation: Dm. Faust et al., THE ACTIVITY OF THE HIGHLY INDUCIBLE MOUSE PHENYLALANINE-HYDROXYLASE GENE PROMOTER IS DEPENDENT UPON A TISSUE-SPECIFIC, HORMONE-INDUCIBLE ENHANCER, Molecular and cellular biology, 16(6), 1996, pp. 3125-3137
LOSS OF SEQUENCE-3' TO THE TESTIS-DETERMINING GENE, SRY, INCLUDING THE Y-PSEUDOAUTOSOMAL BOUNDARY ASSOCIATED WITH PARTIAL TESTICULAR DETERMINATION
Authors: MCELREAVEY K VILAIN E BARBAUX S FUQUA JS FECHNER PY SOULEYREAU N DOCOFENZY M GABRIEL R QUEREUX C FELLOUS M BERKOVITZ GD
Citation: K. Mcelreavey et al., LOSS OF SEQUENCE-3' TO THE TESTIS-DETERMINING GENE, SRY, INCLUDING THE Y-PSEUDOAUTOSOMAL BOUNDARY ASSOCIATED WITH PARTIAL TESTICULAR DETERMINATION, Proceedings of the National Academy of Sciences of the United Statesof America, 93(16), 1996, pp. 8590-8594
PROXIMAL DELETIONS OF THE LONG ARM OF THE Y-CHROMOSOME SUGGEST A CRITICAL REGION ASSOCIATED WITH A SPECIFIC SUBSET OF CHARACTERISTIC TURNERSTIGMATA
Authors: BARBAUX S VILAIN E RAOUL O GILGENKRANTZ S JEANDIDIER E CHADENAS D SOULEYREAU N FELLOUS M MCELREAVEY K
Citation: S. Barbaux et al., PROXIMAL DELETIONS OF THE LONG ARM OF THE Y-CHROMOSOME SUGGEST A CRITICAL REGION ASSOCIATED WITH A SPECIFIC SUBSET OF CHARACTERISTIC TURNERSTIGMATA, Human molecular genetics, 4(9), 1995, pp. 1565-1568
A VIEW ON SEX DETERMINATION IN MAMMALS
Authors: BARBAUX S VILAIN E MCELREAVEY K FELLOUS M
Citation: S. Barbaux et al., A VIEW ON SEX DETERMINATION IN MAMMALS, MS. Medecine sciences, 11(4), 1995, pp. 529-536
TESTICULAR DEVELOPMENT IN AN SRY-NEGATIVE 46,XX INDIVIDUAL HARBORING A DISTAL XP DELETION
Authors: TAR A SOLYOM J GYORVARI B ION A TELVI L BARBAUX S SOULEYREAU N VILAIN E FELLOUS M MCELREAVEY K
Citation: A. Tar et al., TESTICULAR DEVELOPMENT IN AN SRY-NEGATIVE 46,XX INDIVIDUAL HARBORING A DISTAL XP DELETION, Human genetics, 96(4), 1995, pp. 464-468
THE GENETIC-BASIS OF MURINE AND HUMAN SEX DETERMINATION - A REVIEW
Authors: MCELREAVEY K BARBAUX S ION A FELLOUS M
Citation: K. Mcelreavey et al., THE GENETIC-BASIS OF MURINE AND HUMAN SEX DETERMINATION - A REVIEW, Heredity, 75, 1995, pp. 599-611
MUTATIONS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN 46,XY INDIVIDUALS ARE ASSOCIATED WITH A SPECTRUM OF SEX-REVERSED PHENOTYPES
Authors: MCELREAVEY K BARBAUX S VEITIA R FELLOUS M
Citation: K. Mcelreavey et al., MUTATIONS IN THE TESTIS-DETERMINING REGION OF THE Y-CHROMOSOME IN 46,XY INDIVIDUALS ARE ASSOCIATED WITH A SPECTRUM OF SEX-REVERSED PHENOTYPES, American journal of human genetics, 57(4), 1995, pp. 769-769
DELETIONS OF YQ11 ASSOCIATED WITH INFERTILITY, SHORT STATURE AND THE TURNER-SYNDROME - TENTATIVE MAPPING OF A REGION ASSOCIATED WITH TURNERSTIGMATA TO PROXIMAL INTERVAL-5
Authors: MCELREAVEY K BARBAUX S VILAIN E ION R TELVI L FELLOUS M
Citation: K. Mcelreavey et al., DELETIONS OF YQ11 ASSOCIATED WITH INFERTILITY, SHORT STATURE AND THE TURNER-SYNDROME - TENTATIVE MAPPING OF A REGION ASSOCIATED WITH TURNERSTIGMATA TO PROXIMAL INTERVAL-5, Cytogenetics and cell genetics, 67(4), 1994, pp. 391-392
IDENTIFICATION OF A NOVEL MEMBER OF THE PENTRAXIN FAMILY IN XENOPUS-LAEVIS
Authors: SEERY LT SCHOENBERG DR BARBAUX S SHARP PM WHITEHEAD AS
Citation: Lt. Seery et al., IDENTIFICATION OF A NOVEL MEMBER OF THE PENTRAXIN FAMILY IN XENOPUS-LAEVIS, Proceedings - Royal Society. Biological Sciences, 253(1338), 1993, pp. 263-270
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