NORMAL ACTIVITY OF NUCLEOSIDE PHOSPHORYLASE, SUPEROXIDE DISMUTASE AND CATALASE IN SKIN FIBROBLASTS CULTURED FROM ATAXIA-TELANGIECTASIA PATIENTS.ABELIOVICH D; COHEN MM.1978; ISRAEL J. MED. SCI.; ISRAEL; DA. 1978; VOL. 14; NO 2; PP. 284-287; BIBL. 24 REF.Article

GENETICS OF CEREBROTENDINOUS XANTHOMATOSIS (CTX): AN AUTOSOMAL RECESSIVE TRAIT WITH HIGH GENE FREQUENCY IN SEPHARDIM OF MOROCCAN ORIGINBERGINER WM; ABELIOVICH D.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 2; PP. 151-157; BIBL. 17 REF.Article

RADIAL RAY APLASIA AND RENAL ANOMALIES IN FATHER AND SON: A NEW SYNDROMESOFER S; BAR ZIV J; ABELIOVICH D et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 151-157; BIBL. 19 REF.Article

3:1 MEIOTIC DISJUNCTION IN A MOTHER WITH A BALANCED TRANSLOCATION, 46,XX,T(5,14) (P15;Q13) RESULTING IN TERTIARY TRISOMY AND TERTIARY MONOSOMY OFFSPRINGABELIOVICH D; YAGUPSKY P; BASHAN N et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 1; PP. 83-89; BIBL. 33 REF.Article

THE BRANCHIO-OTO-RENAL (BOR) SYNDROME: REPORT OF BILATERAL RENAL AGENESIS IN THREE SIBSCARMI R; BINSHTOCK M; ABELIOVICH D et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 625-627; BIBL. 10 REF.Article

Chromosomal analysis and health status of children conceived to men during or following dibromochloropropane-induced spermatogenic suppressionPOTASHNIK, G; ABELIOVICH, D.Andrologia. 1985, Vol 17, Num 3, pp 291-296, issn 0303-4569Article

KLINEFELTER'S AND TAKAYASU'S SYNDROMES IN ONE PATIENT. A PURE COINCIDENCE.BERGINER VM; PARAN E; HIRSCH M et al.1983; ANGIOLOGY; ISSN 0003-3197; USA; DA. 1983; VOL. 34; NO 3; PP. 170-175; BIBL. 8 REF.Article

Clinical variability of partial duplication 1q: a clinical report and literature reviewROSENTHAL, J; ABELIOVICH, D; CARMI, R et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 787-792, issn 0148-7299Article

BRIEF CLINICAL REPORT: FAMILIAL MIDGUT ANOMALIES - A SPECTRUM OF DEFECTS DUE TO THE SAME CAUSE.CARMI R; ABELIOVICH D; SIPLOVICH L et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 8; NO 4; PP. 443-446; BIBL. 12 REF.Article

MALFORMATION SYNDROME ASSOCIATED WITH SMALL EXTRA CHROMOSOMECARMI R; ABELIOVICH D; BAR ZIV J et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 1; PP. 101-107; BIBL. 13 REF.Article

Loss of Y chromosome : an age-related event or a cytogenetic marker of a malignant clone ?ABELIOVICH, D; YEHUDA, O; BEN-NERIAH, S et al.Cancer genetics and cytogenetics. 1994, Vol 76, Num 1, pp 70-71, issn 0165-4608Article

Preimplantation exclusion of embryos at risk for prion diseasesMEINER, V; WEINBERG, N; SAFRAN, A et al.Neurology. 2006, Vol 66, Num 4, pp 607-608, issn 0028-3878, 2 p.Article

Clinical implications of fluorescence in situ hybridization analysis in 13 chronic myeloid leukemia cases : Ph-negative and variant ph-positiveYEHUDA, O; ABELIOVICH, D; BEN YEHUDA, D et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 2, pp 100-107, issn 0165-4608Article

Genetic testing of breast and ovarian cancer patients : clinical characteristics and hormonal risk modifiersKADURI, L; GIBS, M; HUBERT, A et al.European journal of obstetrics, gynecology, and reproductive biology. 1999, Vol 85, Num 1, pp 75-80, issn 0301-2115Conference Paper

A 28-kb deletion spanning D15S63 (PW71) in five families : A rare neutral variant?BUITING, K; DITTRICH, B; HORSTHEMKE, B et al.American journal of human genetics. 1999, Vol 65, Num 6, pp 1588-1594, issn 0002-9297Article

dup(10q) Lacking α-satellite DNA in bone marrow cells of a patient with acute myeloid leukemiaABELIOVICH, D; YEHUDA, O; BEN-NERIAH, S et al.Cancer genetics and cytogenetics. 1996, Vol 89, Num 1, pp 1-6, issn 0165-4608Article

t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspringABELIOVICH, D; DAGAN, J; LERER, I et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 45-51, issn 0148-7299Article

Prenatal sex diagnosis: testosterone and FSH levels in mid-trimester amniotic fluidsABELIOVICH, D; LEIBERMAN, J. R; TEUERSTEIN, I et al.Prenatal diagnosis. 1984, Vol 4, Num 5, pp 347-353, issn 0197-3851Article

Preimplantation genetic diagnosis for BRCA1/2-a novel clinical experienceSAGI, M; WEINBERG, N; LAUFER, N et al.Prenatal diagnosis. 2009, Vol 29, Num 5, pp 508-513, issn 0197-3851, 6 p.Article

Glutathione-S-transferase Ml, TI and PI polymorphisms, and breast cancer risk, in BRCA1/2 mutation carriersKADOURI, L; KOTE-JARAI, Z; HUBERT, A et al.British journal of cancer. 2008, Vol 98, Num 12, pp 2006-2010, issn 0007-0920, 5 p.Article

Trisomy 2 : Confined placental mosaicism in a fetus with intrauterine growth retardationARIEL, I; LERER, I; YAGEL, S et al.Prenatal diagnosis. 1997, Vol 17, Num 2, pp 180-183, issn 0197-3851Article

Localization of two X-linked mental retardation (XLMR) genes to Xp : MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2BAR-DAVID, S; LERER, I; SARFATY, C. K et al.American journal of medical genetics. 1996, Vol 64, Num 1, pp 83-88, issn 0148-7299Article

Homozygosity for Waardenburg syndromeZLOTOGORA, J; LERER, I; BAR-DAVID, S et al.American journal of human genetics. 1995, Vol 56, Num 5, pp 1173-1178, issn 0002-9297Article

Molecular diagnosis of Prader-Willi syndrome : parent-of-origin dependent methylation sites and non-isotopic detection of (CA)_n dinucleotide repeat polymorphismsLERER, I; MEINER, V; PASHUT-LAVON, I et al.American journal of medical genetics. 1994, Vol 52, Num 1, pp 79-84, issn 0148-7299Article

Jumping translocation in a 17-month-old child with mixed-lineage leukemiaBEN-NERIAH, S; ABRAMOV, A; LERER, I et al.Cancer genetics and cytogenetics. 1991, Vol 56, Num 2, pp 223-229, issn 0165-4608Article