AAAAAA
Results:
1-12
|
Results: 12
Authors:
STRASSBURGER D
KOMAROVSKI D
LAPIDOT Y
ROSENSAFT J
GELMANKOHAN Z
RONEL R
Citation: D. Strassburger et al., THE CORRELATION BETWEEN FISH AND CYTOGENETIC ANALYSIS OF MONONUCLEATED AND MULTINUCLEATED HUMAN ZYGOTES, Human reproduction (Oxford. Print), 13, 1998, pp. 137-137
Authors:
VANDENHEUVEL L
RUITENBEEK W
SMEETS R
GELMANKOHAN Z
ELPELEG O
LOEFFEN J
TRIJBELS F
MARIMAN E
DEBRUIJN D
SMEITINK J
Citation: L. Vandenheuvel et al., DEMONSTRATION OF A NEW PATHOGENIC MUTATION IN HUMAN COMPLEX-I DEFICIENCY - A 5-BP DUPLICATION IN THE NUCLEAR GENE ENCODING THE 18-KD (AQDQ)SUBUNIT, American journal of human genetics, 62(2), 1998, pp. 262-268
Authors:
GEVA D
EZRI T
SZMUK P
GELMANKOHAN Z
SHKLAR BZ
Citation: D. Geva et al., ANESTHESIA FOR HECHT-BEALS-SYNDROME, Paediatric anaesthesia, 7(2), 1997, pp. 178-179
Authors:
GABIS L
GELMANKOHAN Z
MOGILNER M
Citation: L. Gabis et al., MICROCEPHALY DUE TO FETAL BRAIN DISRUPTION SEQUENCE - CASE-REPORT, Journal of perinatal medicine, 25(2), 1997, pp. 213-215
Authors:
GELMANKOHAN Z
ROSENSAFT J
BENHUR H
HABER A
CHEMKE J
Citation: Z. Gelmankohan et al., CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES - A COMPARATIVE-STUDY, Prenatal diagnosis, 16(2), 1996, pp. 165-168
Authors:
RACHMILEWITZ J
ELKIN M
ROSENSAFT J
GELMANKOHAN Z
ARIEL I
LUSTIG O
SCHNEIDER T
GOSHEN R
BIRAN H
DEGROOT N
HOCHBERG A
Citation: J. Rachmilewitz et al., H19 EXPRESSION AND TUMORIGENICITY OF CHORIOCARCINOMA DERIVED CELL-LINES, Oncogene, 11(5), 1995, pp. 863-870
Authors:
GELMANKOHAN Z
CHEMKE J
Citation: Z. Gelmankohan et J. Chemke, PRENATAL-DIAGNOSIS OF SLO SYNDROME, American journal of medical genetics, 56(3), 1995, pp. 288-288
Authors:
ABELIOVICH D
GELMANKOHAN Z
SILVERSTEIN S
LERER I
CHEMKE J
MERIN S
ZLOTOGORA J
Citation: D. Abeliovich et al., FAMILIAL CAFE AU LAIT SPOTS - A VARIANT OF NEUROFIBROMATOSIS TYPE-1, Journal of Medical Genetics, 32(12), 1995, pp. 985-986
Authors:
DAR H
SCHAAP T
BAITOR H
BOROCHOWITZ Z
GELMANKOHAN Z
CHEMKE T
CHAKI R
COHEN H
FALIKBORENSTEIN Z
CHEMKE J
Citation: H. Dar et al., ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OFFOUNDER CHROMOSOMES(), Israel journal of medical sciences, 31(5), 1995, pp. 323-325
Authors:
DROR Y
GELMANKOHAN Z
HAGAI Z
JUSTERREICHER A
NISANIBENCOHEN R
MOGILNER B
Citation: Y. Dror et al., APLASIA-CUTIS-CONGENITA, ELEVATED ALPHA-FETOPROTEIN, AND A DISTINCT AMNIOTIC-FLUID ACETYLCHOLINESTERASE ELECTROPHORETIC BAND, American journal of perinatology, 11(2), 1994, pp. 149-152
Authors:
ELYAKIM S
LERER I
ZLOTOGORA J
SAGI M
GELMANKOHAN Z
MERIN S
ABELIOVICH D
Citation: S. Elyakim et al., NEUROFIBROMATOSIS TYPE-I (NFI) IN ISRAELI FAMILIES - LINKAGE ANALYSISAS A DIAGNOSTIC-TOOL, American journal of medical genetics, 53(4), 1994, pp. 325-334
Authors:
GELMANKOHAN Z
ROSENSAFT J
BENCOHEN RN
CHEMKE J
Citation: Z. Gelmankohan et al., HOMOZYGOSITY FOR INVERSION (2)(P12Q14), Human genetics, 92(4), 1993, pp. 427-427
Risultati:
1-12
|