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Results:
1-24
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Results: 24
Authors:
HOROWITZ M
PASMANIKCHOR M
BOROCHOWITZ Z
FALIKZACCAI T
HELDMANN K
CARMI R
PARVARI R
BEITOR H
GOLDMAN B
PELEG L
LEVYLAHAD E
RENBAUM P
LEGUM S
SHOMRAT R
YEGER H
BENBENISTI D
NAVON R
DROR V
SHOHAT M
MAGAL N
NAVOT N
EYAL N
Citation: M. Horowitz et al., PREVALENCE OF GLUCOCEREBROSIDASE MUTATIONS IN THE ISRAELI ASHKENAZI JEWISH POPULATION, Human mutation, 12(4), 1998, pp. 240-244
Authors:
SCHUFFENHAUER S
LICHTNER P
PEYKARDERAKHSHANDEH P
MURKEN J
HAAS OA
BACK E
WOLFF G
ZABEL B
BARISIC I
RAUCH A
BOROCHOWITZ Z
DALLAPICCOLA B
ROSS M
MEITINGER T
Citation: S. Schuffenhauer et al., DELETION MAPPING ON CHROMOSOME 10P AND DEFINITION OF A CRITICAL REGION FOR THE 2ND DIGEORGE-SYNDROME LOCUS (DGS2), European journal of human genetics, 6(3), 1998, pp. 213-225
Authors:
ZACCAI F
TZIPORA C
SHACHAK E
COHN N
BADARNY S
HONIGMANN S
BOROCHOWITZ Z
GILADI N
Citation: F. Zaccai et al., PRIMARY TORSION DYSTONIA, OPPENHEIMS TYPE - MOLECULAR CHARACTERIZATION OF THE DISEASE AMONG DIFFERENT ETHNIC-GROUPS IN ISRAEL, European journal of human genetics, 6, 1998, pp. 4019-4019
Authors:
BOROCHOWITZ Z
SABO E
MISSELEVITCH I
BOSS JH
Citation: Z. Borochowitz et al., AUTOSOMAL-RECESSIVE OMODYSPLASIA - PRENATAL-DIAGNOSIS AND HISTOMORPHOMETRIC ASSESSMENT OF THE PHYSEAL PLATES OF THE LONG BONES, American journal of medical genetics, 76(3), 1998, pp. 238-244
Authors:
PAZNEKAS WA
CUNNINGHAM ML
HOWARD TD
KORF BR
LIPSON MH
GRIX AW
FEINGOLD M
GOLDBERG R
BOROCHOWITZ Z
ALECK K
MULLIKEN J
YIN MF
JABS EW
Citation: Wa. Paznekas et al., GENETIC-HETEROGENEITY OF SAETHRE-CHOTZEN-SYNDROME, DUE TO TWIST AND FGFR MUTATIONS, American journal of human genetics, 62(6), 1998, pp. 1370-1380
Authors:
BOROCHOWITZ Z
SHALEV SA
YEHUDAI I
BAREL H
DAR H
TIROSH E
Citation: Z. Borochowitz et al., DELETION (4)(Q33-]QTER) - A CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of child neurology, 12(5), 1997, pp. 335-337
Authors:
KUGELMAN A
HADAD B
BENDAVID J
PODOSHIN L
BOROCHOWITZ Z
BADER D
Citation: A. Kugelman et al., PREAURICULAR TAGS AND PITS IN THE NEWBORN - THE ROLE OF HEARING TESTS, Acta paediatrica, 86(2), 1997, pp. 170-172
Authors:
SHAPIRA M
DAR H
BAREL H
BARNITZAN N
EVEN L
BOROCHOWITZ Z
Citation: M. Shapira et al., INHERITED INVERTED DUPLICATION OF X-CHROMOSOME IN A MALE - REPORT OF A PATIENT AND REVIEW OF THE LITERATURE, American journal of medical genetics, 72(4), 1997, pp. 409-414
Authors:
FALIKZACCAI TC
SHACHAK E
COHEN N
HONIGMAN S
BOROCHOWITZ Z
GILADI N
Citation: Tc. Falikzaccai et al., IDIOPATHIC TORSION DYSTONIA (ITD) - MOLECULAR-GENETIC ANALYSIS OF ASHKENAZI JEWS AND SEPHARDIC JEWS IN ISRAEL, Neurology, 48(3), 1997, pp. 6087-6087
Authors:
FALIKZACCAI TC
SHACHAK E
YALON M
LIS Z
BOROCHOWITZ Z
MACPHERSON JN
NELSON DL
EICHLER EE
Citation: Tc. Falikzaccai et al., PREDISPOSITION TO THE FRAGILE-X-SYNDROME IN JEWS OF TUNISIAN DESCENT IS DUE TO THE ABSENCE OF AGG INTERRUPTIONS ON A RARE MEDITERRANEAN HAPLOTYPE, American journal of human genetics, 60(1), 1997, pp. 103-112
Authors:
GERSHONIBARUCH R
MANDEL H
EL HB
BARNIZAN N
BOROCHOWITZ Z
DAR H
Citation: R. Gershonibaruch et al., INTERSTITIAL DELETION (6)Q13Q15, American journal of medical genetics, 62(4), 1996, pp. 345-347
Authors:
SHALEV SA
DAR H
BAREL H
BOROCHOWITZ Z
Citation: Sa. Shalev et al., UPPER-LIMB MALFORMATIONS IN CHROMOSOME 22Q11 DELETIONS, American journal of medical genetics, 62(3), 1996, pp. 302-302
Authors:
DAVID M
ISRAEL N
MERKSAMER R
BARNIZAN N
BOROCHOWITZ Z
BAREL H
YEHUDAI I
DAR H
Citation: M. David et al., VERY-LOW MATERNAL SERUM UNCONJUGATED ESTRIOL AND PRENATAL-DIAGNOSIS OF STEROID SULFATASE DEFICIENCY, Fetal diagnosis and therapy, 10(2), 1995, pp. 76-80
Authors:
FALIKBORENSTEIN TC
HOLMES SA
BOROCHOWITZ Z
LEVIN A
ROSENMANN A
SPRITZ RA
Citation: Tc. Falikborenstein et al., DNA-BASED CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF TYROSINASE-NEGATIVE OCULOCUTANEOUS ALBINISM (OCA1A), Prenatal diagnosis, 15(4), 1995, pp. 345-349
Authors:
BOROCHOWITZ Z
BARAK M
HERSHKOWITZ S
Citation: Z. Borochowitz et al., NOSOLOGY OF OMODYSPLASIA, American journal of medical genetics, 58(4), 1995, pp. 377-377
Authors:
SHOHAT M
LEGUM C
ROMEM Y
BOROCHOWITZ Z
BACH G
GOLDMAN B
Citation: M. Shohat et al., DOWN-SYNDROME PREVENTION PROGRAM IN A POPULATION WITH AN OLDER MATERNAL AGE, Obstetrics and gynecology, 85(3), 1995, pp. 368-373
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:
FALIKBORENSTEIN TC
YALON M
SHACHAK L
DAR C
BOROCHOWITZ Z
NELSON DL
MACPHERSON JN
EICHLER EE
Citation: Tc. Falikborenstein et al., LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS, American journal of human genetics, 57(4), 1995, pp. 1218-1218
Authors:
SHAPIRA M
BOROCHOWITZ Z
BAREL H
DAR H
ETZIONI A
LORBER A
Citation: M. Shapira et al., DELETION OF THE SHORT ARM, OF CHROMOSOME-10 (10P13) - REPORT OF A PATIENT AND REVIEW, American journal of medical genetics, 52(1), 1994, pp. 34-38
Authors:
BRONSTEIN M
REICHLER A
BOROCHOWITZ Z
BEJAR J
DRUGAN A
Citation: M. Bronstein et al., EARLY PRENATAL-DIAGNOSIS OF POLYCYSTIC PANCREAS WITH NARROW THORAX AND SHORT LIMB DWARFISM, American journal of medical genetics, 49(1), 1994, pp. 6-9
Authors:
BOROCHOWITZ Z
PAVONE L
MAZOR G
RIZZO R
DAR H
Citation: Z. Borochowitz et al., FACIO-CUTANEOUS-SKELETAL SYNDROME - NEW NOSOLOGICAL ENTITY OR COSTELLO SYNDROME, American journal of medical genetics, 47(2), 1993, pp. 173-173
Authors:
ZLOTOGORA J
FUKS A
BOROCHOWITZ Z
TAL Y
Citation: J. Zlotogora et al., KOHLSCHUTTER-TONZ SYNDROME - EPILEPSY, DEMENTIA, AND AMELOGENESIS-IMPERFECTA, American journal of medical genetics, 46(4), 1993, pp. 453-454
Authors:
BOROCHOWITZ Z
Citation: Z. Borochowitz, SHORT STATURE, METAPHYSEAL INFRACTIONS, WORMIAN BONES, SHORT FINGERS AND SEVERE OSTEOPENIA - A RATHER NEW FAMILIAL AUTOSOMAL RECESSIVE BONEDYSPLASIA, American journal of human genetics, 53(3), 1993, pp. 408-408
Authors:
ZIV Y
FRYDMAN M
LANGE E
ZELNIK N
ROTMAN G
JULIER C
JASPERS NGJ
DAGAN Y
ABELIOVICZ D
DAR H
BOROCHOWITZ Z
LATHROP M
GATTI RA
SHILOH Y
Citation: Y. Ziv et al., ATAXIA-TELANGIECTASIA - LINKAGE ANALYSIS IN HIGHLY INBRED ARAB AND DRUZE FAMILIES AND DIFFERENTIATION FROM AN ATAXIA-MICROCEPHALY-CATARACT SYNDROME, Human genetics, 88(6), 1992, pp. 619-626
Risultati:
1-24
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