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Results: 1-7 |
Results: 7
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
THE FRAGILE-X-SYNDROME IS STILL UNDERDIAG NOSED - EFFICACY OF MOLECULAR TESTING IN MENTALLY-RETARDED PROBANDS
Authors: COSSEE M MOUTOU C BIANCALANA V BOUIX JC PLESSIS G DELOBEL B CROQUETTE MF GILGENKRANTZ S LAMBERT JC MALPUECH G STOLL C LANOE JL PECHEVIS M MANDEL JL
Citation: M. Cossee et al., THE FRAGILE-X-SYNDROME IS STILL UNDERDIAG NOSED - EFFICACY OF MOLECULAR TESTING IN MENTALLY-RETARDED PROBANDS, Archives de pediatrie, 4(3), 1997, pp. 227-236
SEVERE MANIFESTATIONS IN CARRIER FEMALES IN X-LINKED RETINITIS-PIGMENTOSA
Authors: SOUIED E SEGUES B GHAZI I ROZET JM CHATELIN S GERBER S PERRAULT I MICHELAWAD A BRIARD ML PLESSIS G DUFIER JL MUNNICH A KAPLAN J
Citation: E. Souied et al., SEVERE MANIFESTATIONS IN CARRIER FEMALES IN X-LINKED RETINITIS-PIGMENTOSA, Journal of Medical Genetics, 34(10), 1997, pp. 793-797
SCALP DEFECT, ABSENCE OF NIPPLES, EAR ANOMALIES, RENAL HYPOPLASIA - ANOTHER CASE OF FINLAY-MARKS-SYNDROME
Authors: PLESSIS G LETREUST M LEMERRER M
Citation: G. Plessis et al., SCALP DEFECT, ABSENCE OF NIPPLES, EAR ANOMALIES, RENAL HYPOPLASIA - ANOTHER CASE OF FINLAY-MARKS-SYNDROME, Clinical genetics, 52(4), 1997, pp. 231-234
TRISOMY-18 MOSAICISM IN A MILDLY RETARDED BOY WITH POSTNATAL OVERGROWTH
Authors: PLESSIS G LETREUST M LEMAIRE F MAUGARD T CAU D
Citation: G. Plessis et al., TRISOMY-18 MOSAICISM IN A MILDLY RETARDED BOY WITH POSTNATAL OVERGROWTH, Annales de genetique, 40(4), 1997, pp. 235-237
NO EVIDENCE OF GENETIC-HETEROGENEITY IN DOMINANT OPTIC ATROPHY
Authors: BONNEAU D SOUIED E GERBER S ROZET JM DHAENS E JOURNEL H PLESSIS G WEISSENBACH J MUNNICH A KAPLAN J
Citation: D. Bonneau et al., NO EVIDENCE OF GENETIC-HETEROGENEITY IN DOMINANT OPTIC ATROPHY, Journal of Medical Genetics, 32(12), 1995, pp. 951-953
MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3
Authors: PUISSANT H MALINGE MC LARGETPIET A MARTIN D CHAUVEAU P ODENT S PLESSIS G PARENT P LEMAREC B LARGETPIET L
Citation: H. Puissant et al., MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3, American journal of medical genetics, 53(4), 1994, pp. 370-373
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