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Results: 1-7 |
Results: 7
46,XY COMPLETE GONADAL-DYSGENESIS (SYWERS-SYNDROME) AND 46,XY PARTIALGONADAL-DYSGENESIS ASSOCIATED WITH DELETIONS OF 9P
Authors: VEITIA R GONCALVES J SILVA M RODRIGUES JC BOIEIRO F MARQUES R LAVINHA J CASPURRO M NUNES M RAPPAPORT R THIBAUD E JAUBERT F FELLOUS M MCELREAVEY K
Citation: R. Veitia et al., 46,XY COMPLETE GONADAL-DYSGENESIS (SYWERS-SYNDROME) AND 46,XY PARTIALGONADAL-DYSGENESIS ASSOCIATED WITH DELETIONS OF 9P, European journal of human genetics, 6, 1998, pp. 1098-1098
OVARIAN-FUNCTION AFTER BONE-MARROW TRANSPLANTATION DURING CHILDHOOD
Authors: THIBAUD E RODRIGUEZMACIAS K TRIVIN C ESPEROU H MICHON J BRAUNER R
Citation: E. Thibaud et al., OVARIAN-FUNCTION AFTER BONE-MARROW TRANSPLANTATION DURING CHILDHOOD, Bone marrow transplantation, 21(3), 1998, pp. 287-290
SWYER-SYNDROME AND 46,XY PARTIAL GONADAL-DYSGENESIS ASSOCIATED WITH 9P DELETIONS IN THE ABSENCE OF MONOSOMY-9P SYNDROME
Authors: VEITIA RA NUNES M QUINTANAMURCI L RAPPAPORT R THIBAUD E JAUBERT E FELLOUS M MCELREAVEY K GONCALVES J SILVA M RODRIGUES JC CASPURRO M BOIEIRO F MARQUES R LAVINHA J
Citation: Ra. Veitia et al., SWYER-SYNDROME AND 46,XY PARTIAL GONADAL-DYSGENESIS ASSOCIATED WITH 9P DELETIONS IN THE ABSENCE OF MONOSOMY-9P SYNDROME, American journal of human genetics, 63(3), 1998, pp. 901-905
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
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
PRIMARY AMENORRHEA AS THE FIRST MANIFESTA TION OF A CONGENITAL HYDROCEPHALUS
Authors: THIBAUD D THIBAUD E LANDRIEU P ZERAH M
Citation: D. Thibaud et al., PRIMARY AMENORRHEA AS THE FIRST MANIFESTA TION OF A CONGENITAL HYDROCEPHALUS, Archives de pediatrie, 3(11), 1996, pp. 1099-1101
XY GONADAL-DYSGENESIS AND SRY
Authors: BOUCEKKINE C VILAIN E MCELREAVEY K JAUBERT F BRAUNER R THIBAUD E BATTIN J TOUBLANC JE KUCHERIA K CHAABOUNI S ROBEL P GOMPEL A JOSEPH MG LAMBERT JC LORTATJACOB S NIHOULFEKETE C NIVELON JL SCHAISON G RAPPAPORT R VEKEMANS M VIDEAU M COSTA JM FELLOUS M
Citation: C. Boucekkine et al., XY GONADAL-DYSGENESIS AND SRY, Annales d'Endocrinologie, 54(5), 1993, pp. 315-321
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