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Results:
1-11
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Results: 11
Authors:
GUICHET A
BRIAULT S
MORAINE C
Citation: A. Guichet et al., HIGH-RESOLUTION CHROMOSOME ANALYSIS AND IN-SITU HYBRIDIZATION ON AMNIOTIC-FLUID FOR DIAGNOSIS OF A CRYPTIC TRANSLOCATION, Prenatal diagnosis, 18(4), 1998, pp. 399-403
Authors:
BILLUART P
BIENVENU T
RONCE N
DESPORTES V
VINET MC
ZEMNI R
CROLLIUS HR
CARRIE A
FAUCHEREAU F
CHERRY M
BRIAULT S
HAMEL B
FRYNS JP
BELDJORD C
KAHN A
MORAINE C
CHELLY J
Citation: P. Billuart et al., OLIGOPHRENIN-1 ENCODES A RHOGAP PROTEIN INVOLVED IN X-LINKED MENTAL-RETARDATION, Nature, 392(6679), 1998, pp. 923-926
Authors:
GUICHET A
BRIAULT S
LEMERRER M
MORAINE C
Citation: A. Guichet et al., ARE T(X-Y) (P22-Q11) TRANSLOCATIONS IN FEMALES FREQUENTLY ASSOCIATED WITH MADELUNG DEFORMITY, Clinical dysmorphology, 6(4), 1997, pp. 341-345
Authors:
GUICHET A
BRIAULT S
PARINGAUX C
Citation: A. Guichet et al., PRENATAL-DIAGNOSIS OF 45,X 46,XY MOSAICISM WITH ULTRASOUND ABNORMALITY OF THE KIDNEYS AND GOOD OUTCOME FOR A MALE CHILD/, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 153-153
Authors:
BRIAULT S
HILL R
SHRIMPTON A
ZHU DP
TILL M
RONCE N
MARGARITTEJEANNIN P
BARAITSER M
MIDDLETONPRICE H
MALCOLM S
THOMPSON E
HOO J
WILSON G
ROMANO C
GUICHET A
PEMBREY M
FONTES M
POUSTKA A
MORAINE C
Citation: S. Briault et al., A GENE FOR FG-SYNDROME MAPS IN THE XQ12-Q21.31 REGION, American journal of medical genetics, 73(1), 1997, pp. 87-90
Authors:
BRIAULT S
VILLARD L
ODENT S
LUCAS J
RONCE N
TOUTAIN A
GUICHET A
LEMERRER M
TURLEAU C
MUNNICH A
FONTES M
MORAINE CL
Citation: S. Briault et al., PHYSICAL MAPPING OF THE BREAKPOINTS OF AN X-CHROMOSOME PARACENTRIC INVERSION INV(X) (Q11Q28) WHICH COSEGRATES WITH THE FG SYNDROME IN A FRENCH FAMILY, American journal of medical genetics, 64(1), 1996, pp. 20-20
Authors:
RAYNAUD M
GENDROT C
DESSAY B
MONCLA A
AYRAULT AD
MOIZARD MP
TOUTAIN A
BRIAULT S
VILLARD L
RONCE N
MORAINE C
Citation: M. Raynaud et al., X-LINKED MENTAL-RETARDATION WITH NEONATAL HYPOTONIA IN A FRENCH FAMILY (MRX15) - GENE ASSIGNMENT TO XP11.22-XP21.1, American journal of medical genetics, 64(1), 1996, pp. 97-106
Authors:
GUICHET A
BRIAULT S
MORAINE C
TURLEAU C
Citation: A. Guichet et al., TRISOMY-X - ACLF SOCIATION-DES-CYTOGENETICIENS-DE-LANGUE-FRANCAISE) RETROSPECTIVE STUDY, Annales de genetique, 39(3), 1996, pp. 117-122
Authors:
GUICHET A
BRIAULT S
TOUTAIN A
PAILLET C
DESCAMPS P
PIERRE F
BODY G
MORAINE CL
Citation: A. Guichet et al., PRENATAL-DIAGNOSIS OF TRISOMY-8 MOSAICISM IN CVS AFTER ABNORMAL ULTRASOUND FINDINGS AT 12 WEEKS, Prenatal diagnosis, 15(8), 1995, pp. 769-772
Authors:
GENDROT C
RONCE N
TOUTAIN A
MOIZARD MP
MUH JP
RAYNAUD M
DOURLENS J
BRIAULT S
MORAINE C
Citation: C. Gendrot et al., X-LINKED MENTAL-RETARDATION EXHIBITING LINKAGE TO DXS255 AND PGKP1 - A NEW MRX FAMILY (MRX14) WITH LOCALIZATION IN THE PERICENTROMERIC REGION, Clinical genetics, 45(3), 1994, pp. 145-153
Authors:
HOUDAYER C
TOUTAIN A
RONCE N
LEFORT G
SARDA P
TAIB J
BRIAULT S
LAMBERT JC
MORAINE C
Citation: C. Houdayer et al., X-LINKED ALPHA-THALASSEMIA MENTAL RETARDATION SYNDROME - LINKAGE ANALYSIS IN A NEW FAMILY FURTHER SUPPORTS LOCALIZATION IN PROXIMAL XQ/, Annales de genetique, 36(4), 1993, pp. 194-199
Risultati:
1-11
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