Authors:
BARSADE RB
KRUGLIKOVA A
MODAN B
GAK E
HIRSHYECHEZKEL G
THEODOR L
NOVIKOV I
GERSHONIBARUCH R
RISEL S
PAPA MZ
BENBARUCH G
FRIEDMAN E
Citation: Rb. Barsade et al., THE 185DELAG BRCA1 MUTATION ORIGINATED BEFORE THE DISPERSION OF JEWS IN THE DIASPORA AND IS NOT LIMITED TO ASHKENAZIM, Human molecular genetics, 7(5), 1998, pp. 801-805
Citation: N. Shehadeh et al., CONGENITAL DIABETES IN AN INFANT WITH TRISOMY-21, Journal of pediatric endocrinology & metabolism, 11(4), 1998, pp. 575-576
Authors:
ETZIONI A
GERSHONIBARUCH R
POLLACK S
SHEHADEH N
Citation: A. Etzioni et al., LEUKOCYTE ADHESION DEFICIENCY TYPE-II - LONG-TERM FOLLOW-UP, Journal of allergy and clinical immunology, 102(2), 1998, pp. 323-324
Authors:
KARSAN A
CORNEJO CJ
WINN RK
SCHWARTZ BR
WAY W
LANNIR N
GERSHONIBARUCH R
ETZIONI A
OCHS HD
HARLAN JM
Citation: A. Karsan et al., LEUKOCYTE ADHESION DEFICIENCY TYPE-II IS A GENERALIZED DEFECT OF DE-NOVO GDP-FUCOSE BIOSYNTHESIS - ENDOTHELIAL-CELL FUCOSYLATION IS NOT REQUIRED FOR NEUTROPHIL ROLLING ON HUMAN NONLYMPHOID ENDOTHELIUM, The Journal of clinical investigation, 101(11), 1998, pp. 2438-2445
Authors:
FRIEDMAN E
BRUCHIM RB
KRUGLIKOVA A
RISEL S
LEVYLAHAD E
HALLE D
BARON E
GERSHONIBARUCH R
DAGAN E
KEPTEN I
PERETZ T
LERER I
WIENBERG N
SHUSHAN A
ABELIOVICH D
Citation: E. Friedman et al., DOUBLE HETEROZYGOTES FOR THE ASHKENAZI FOUNDER MUTATIONS IN BRCA1 ANDBRCA2 GENES, American journal of human genetics, 63(4), 1998, pp. 1224-1227
Authors:
NEUHAUSEN SL
GODWIN AK
GERSHONIBARUCH R
SCHUBERT E
GARBER J
STOPPALYONNET D
OLAH E
CSOKAY B
SEROVA O
LALLOO F
OSORIO A
STRATTON M
OFFIT K
BOYD J
CALIGO MA
SCOTT RJ
SCHOFIELD A
TEUGELS E
SCHWAB M
CANNONALBRIGHT L
BISHOP T
EASTON D
BENITEZ J
KING MC
PONDER BAJ
WEBER B
DEVILEE P
BORG A
NAROD SA
GOLDGAR D
Citation: Sl. Neuhausen et al., HAPLOTYPE AND PHENOTYPE ANALYSIS OF 9 RECURRENT BRCA2 MUTATIONS IN 111 FAMILIES - RESULTS OF AN INTERNATIONAL STUDY, American journal of human genetics, 62(6), 1998, pp. 1381-1388
Authors:
GERSHONIBARUCH R
DAGAN E
KEPTEN I
FREID G
Citation: R. Gershonibaruch et al., CO-SEGREGATION OF BRCA1 185DELAG MUTATION AND BRCA2 6174DELT IN ONE SINGLE-FAMILY, European journal of cancer, 33(13), 1997, pp. 2283-2284
Citation: R. Gershonibaruch et al., ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME AND HYPOTHALAMOPITUITARY INSUFFICIENCY, American journal of medical genetics, 68(2), 1997, pp. 168-172
Authors:
DAGAN E
KEPTEN I
AKKERMAN T
FRIED G
BEK D
GERSHONIBARUCH R
Citation: E. Dagan et al., PATTERNS OF MORBIDITY IN HIGHLY SELECTED PATIENTS WITH BREAST AND OR OVARIAN-CANCER CARRIERS OF THE 3 ANCIENT MUTATIONS, 185DELAG AND 5382INSC IN BRCA1 AND 6174DELT IN BRCA2/, American journal of human genetics, 61(4), 1997, pp. 337-337
Authors:
LEVYLAHAD E
GERSHONIBARUCH R
SAGI M
ORRURTREGER A
BENYEHUDA A
DAGAN E
BARSADE R
LAHAD A
HALLE D
PERETZ T
FRIEDMAN E
Citation: E. Levylahad et al., DIRECTLY DERIVED PENETRANCE ESTIMATES FOR THE FOUNDER BRCA1 BRCA2 MUTATIONS IN JEWS - THE ISRAELI CONSORTIUM ON HEREDITARY BREAST-CANCER/, American journal of human genetics, 61(4), 1997, pp. 389-389
Authors:
DAGAN E
KEPTEN I
AKERMAN T
FRIED G
BEK D
GERSHONIBARUCH R
BADARNA K
Citation: E. Dagan et al., CARRIER FREQUENCY OF THE G47D MUTATION IN THE TYROSINASE GENE IN INDIVIDUALS OF JEWISH MOROCCAN ORIGIN, American journal of human genetics, 61(4), 1997, pp. 1169-1169
Citation: R. Gershonibaruch et D. Zekaria, DELETION (13)(Q22) WITH MULTIPLE CONGENITAL-ANOMALIES, HYDRANENCEPHALY AND PENOSCROTAL TRANSPOSITION, Clinical dysmorphology, 5(4), 1996, pp. 289-294
Citation: R. Gershonibaruch et R. Leibo, APLASIA-CUTIS-CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION IN 2 SIBS - A NEW AUTOSOMAL RECESSIVE DISORDER, American journal of medical genetics, 61(1), 1996, pp. 42-44
Authors:
MILLS K
MANDEL H
MONTEMAGNO R
SOOTHILL P
GERSHONIBARUCH R
CLAYTON PT
Citation: K. Mills et al., FIRST TRIMESTER PRENATAL-DIAGNOSIS OF SMITH-LEMLI-OPITZ SYNDROME (7-DEHYDROCHOLESTEROL REDUCTASE DEFICIENCY), Pediatric research, 39(5), 1996, pp. 816-819
Authors:
DRUGAN A
VADAS A
SUJOV P
GERSHONIBARUCH R
Citation: A. Drugan et al., MARKEDLY ELEVATED ALPHA-FETOPROTEIN AND POSITIVE ACETYLCHOLINESTERASEIN AMNIOTIC-FLUID FROM A PREGNANCY AFFECTED WITH DYSTROPHIC EPIDERMOLYSIS-BULLOSA, Fetal diagnosis and therapy, 10(1), 1995, pp. 37-40
Authors:
GILHAR A
GERSHONIBARUCH R
MARGOLIS A
BENDERLY A
BRANDES JM
Citation: A. Gilhar et al., DOPA REACTION OF FETAL MELANOCYTES BEFORE AND AFTER SKIN TRANSPLANTATION ON TO NUDE-MICE, British journal of dermatology, 133(6), 1995, pp. 884-889
Citation: R. Gershonibaruch et al., ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING (EEC) SYNDROME AND HYPOTHALAMIC-PITUITARY INSUFFICIENCY, American journal of human genetics, 57(4), 1995, pp. 492-492
Authors:
GERSHONIBARUCH R
EPSTEIN R
TZISCHINSKY O
LAVIE P
BRANDES JM
Citation: R. Gershonibaruch et al., ACTIGRAPHIC HOME-MONITORING OF THE SLEEP PATTERNS OF IN-VITRO FERTILIZATION CHILDREN AND THEIR MATCHED CONTROLS, Developmental Medicine and Child Neurology, 36(7), 1994, pp. 639-645
Authors:
PRICE TH
OCHS HD
GERSHONIBARUCH R
HARLAN JM
ETZIONI A
Citation: Th. Price et al., IN-VIVO NEUTROPHIL AND LYMPHOCYTE FUNCTION STUDIES IN A PATIENT WITH LEUKOCYTE ADHESION DEFICIENCY TYPE-II, Blood, 84(5), 1994, pp. 1635-1639
Authors:
GERSHONIBARUCH R
ROSENMANN A
DROETTO S
HOLMES S
TRIPATHI RK
SPRITZ RA
Citation: R. Gershonibaruch et al., MUTATIONS OF THE TYROSINASE GENE IN PATIENTS WITH OCULOCUTANEOUS ALBINISM FROM VARIOUS ETHNIC-GROUPS IN ISRAEL, American journal of human genetics, 54(4), 1994, pp. 586-594