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Results: 1-8 |
Results: 8
NO FOUNDER EFFECT DETECTED IN JEWISH ASHKENAZI PATIENTS WITH FRAGILE-X-SYNDROME
Authors: PESSO R BARKAI G RAVIA Y GAK E FRYDMAN M GOLDMAN B FRIEDMAN E
Citation: R. Pesso et al., NO FOUNDER EFFECT DETECTED IN JEWISH ASHKENAZI PATIENTS WITH FRAGILE-X-SYNDROME, Human genetics, 101(2), 1997, pp. 186-189
DETECTION OF CHROMOSOMAL ABERRATION IN SPONTANEOUSLY MISSED ABORTUSESBY COMPARATIVE GENOMIC HYBRIDIZATION
Authors: DANIELY M AVIRAMGOLDRING A RAVIA Y BARKAI G GOLDMAN B
Citation: M. Daniely et al., DETECTION OF CHROMOSOMAL ABERRATION IN SPONTANEOUSLY MISSED ABORTUSESBY COMPARATIVE GENOMIC HYBRIDIZATION, American journal of human genetics, 61(4), 1997, pp. 688-688
ANALYSIS OF FETAL CELLS IN MATERNAL BLOOD BY PCR
Authors: RAVIA Y NAKASH Y SHAKI R BARKAI G GOLDMAN B
Citation: Y. Ravia et al., ANALYSIS OF FETAL CELLS IN MATERNAL BLOOD BY PCR, American journal of human genetics, 57(4), 1995, pp. 1668-1668
X-LINKED RECESSIVE PRIMARY RETINAL DYSPLASIA IS LINKED TO THE NORRIE DISEASE LOCUS
Authors: RAVIA Y BRAIERGOLDSTEIN O BATMIRIAM KM ERLICH S BARKAI G GOLDMAN B
Citation: Y. Ravia et al., X-LINKED RECESSIVE PRIMARY RETINAL DYSPLASIA IS LINKED TO THE NORRIE DISEASE LOCUS, Human molecular genetics, 2(8), 1993, pp. 1295-1297
MARFAN-SYNDROME - EVIDENCE FOR FOUNDER CHROMOSOMES IN ASHKENAZI JEWS
Authors: RAVIA Y SHOR D REZNIK H GOLDMAN B
Citation: Y. Ravia et al., MARFAN-SYNDROME - EVIDENCE FOR FOUNDER CHROMOSOMES IN ASHKENAZI JEWS, American journal of human genetics, 53(3), 1993, pp. 199-199
DELETION OF PART OF THE DNA ENCODING THE HUMAN PROTEIN-TYROSINE-PHOSPHATASE LAR IN HUMAN TUMORS
Authors: WEINSTEIN M KARASIK A KANETY H PAPA MZ GOLDMAN B RAVIA Y
Citation: M. Weinstein et al., DELETION OF PART OF THE DNA ENCODING THE HUMAN PROTEIN-TYROSINE-PHOSPHATASE LAR IN HUMAN TUMORS, American journal of human genetics, 53(3), 1993, pp. 385-385
VELO-CARDIO-FACIAL SYNDROME (VCFS) - CLINICAL-STUDIES IN 27 PATIENTS AND PRELIMINARY-RESULTS OF MOLECULAR ANALYSIS
Authors: FRYDMAN M FINKELSTEIN Y RAVIA Y SCAMBLER PJ GOLDMAN B
Citation: M. Frydman et al., VELO-CARDIO-FACIAL SYNDROME (VCFS) - CLINICAL-STUDIES IN 27 PATIENTS AND PRELIMINARY-RESULTS OF MOLECULAR ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 435-435
SCREENING FOR FRAGILE-X MUTATION IN MENTALLY-RETARDED INDIVIDUALS
Authors: RAVIA Y PESSO R BRAIERGOLDSTEIN O BRAND N BARKAI G GOLDMAN B
Citation: Y. Ravia et al., SCREENING FOR FRAGILE-X MUTATION IN MENTALLY-RETARDED INDIVIDUALS, American journal of human genetics, 53(3), 1993, pp. 1502-1502
Risultati: 1-8 |