Generalized chondrodysplasie punctata with shortness of humeri and brachymetacarpy : humero-metacarpal (HM) type : variation or heterogeneity ?BOROCHOWITZ, Z.American journal of medical genetics. 1991, Vol 41, Num 4, pp 417-422, issn 0148-7299Conference Paper

A HEMODYNAMIC COMPLICATION OF VERAPAMIL THERAPY IN A NEONATEABINADER E; BOROCHOWITZ Z; BERGER A et al.1981; HELV. PAEDIATR. ACTA; ISSN 0018-022X; CHE; DA. 1981; VOL. 36; NO 5; PP. 451-455; ABS. GER/FRE; BIBL. 10 REF.Article

LOW-DOSE CONTINUOUS INTRAVENOUS INFUSION OF INSULIN ON THE FIRST DAY OF LIFE IN A DIABETIC KETOACIDOTIC NEWBORNABEND M; HOCHBERG Z; BOROCHOWITZ Z et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 4; PP. 345; BIBL. 5 REF.Article

Sleep apnea in fragile X syndromeTIROSH, E; BOROCHOWITZ, Z.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 124-127, issn 0148-7299Article

BILIRUBIN AND PROTEIN CONCENTRATION IN CORD BLOOD AFTER SPONTANEOUS VERSUS INDUCED LABOR. CORRELATION TO NEONATAL HYPERBILIRUBINEMIAGRANAT M; BOROCHOWITZ Z; BERGER A et al.1981; J. PERINAT. MED.; ISSN 0300-5577; DEU; DA. 1981; VOL. 9; NO 1; PP. 27-34; ABS. GER/FRE; BIBL. 24 REF.Article

Familial congenital micromelic dysplasia with dislocation of radius and distinct face : a new skeletal dysplasia syndromeBOROCHOWITZ, Z; BARAK, M; HERSHKOWITZ, S et al.American journal of medical genetics. 1991, Vol 39, Num 1, pp 91-96, issn 0148-7299Article

Familial recurrent dislocation of patella with autosomal dominant mode of inheritanceBOROCHOWITZ, Z; SOUDRY, M; MENDES, D. G et al.Clinical genetics. 1988, Vol 33, Num 1, pp 1-4, issn 0009-9163Article

Spondylometaphyseal dysplasia: further heterogeneityBOROCHOWITZ, Z; BERANT, M; KRISTAL, H et al.Skeletal radiology. 1988, Vol 17, Num 3, pp 181-186, issn 0364-2348Article

Familial congenital fiber type disproportion (CFTD) with an autosomal recessive inheritanceJAFFE, M; SHAPIRA, J; BOROCHOWITZ, Z et al.Clinical genetics. 1988, Vol 33, Num 1, pp 33-37, issn 0009-9163Article

Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs : a lethal new syndromeBOROCHOWITZ, Z; GLICK, B; BLAZER, S et al.Journal of medical genetics. 1991, Vol 28, Num 5, pp 345-348, issn 0022-2593Article

Transient methemoglobinemia with acidosis and hyperchloremia in infantsLANIR, A; BOROCHOWITZ, Z; KAPLAN, T et al.The American journal of pediatric hematology/oncology. 1986, Vol 8, Num 4, pp 353-355, issn 0192-8562Article

Kohlschütter-Tönz syndrome : epilepsy, dementia, and amelogenesis imperfectaZLOTOGORA, J; FUKS, A; BOROCHOWITZ, Z et al.American journal of medical genetics. 1993, Vol 46, Num 4, pp 453-454, issn 0148-7299Article

Diagnostic approach to the etiology of mental retardationJAFFE, M; BOROCHOWITZ, Z; DAR, H et al.Israel journal of medical sciences. 1984, Vol 20, Num 2, pp 136-140, issn 0021-2180Article

Osteosclerosis, hypoplastic nose, and proptosis (Raine syndrome) : Further delineationSHALEV, S. A; SHALEV, E; REICH, D et al.American journal of medical genetics. 1999, Vol 86, Num 3, pp 274-277, issn 0148-7299Article

Autosomal-recessive omodysplasia : Prenatal diagnosis and histomorphometric assessment of the physeal plates of the long bonesBOROCHOWITZ, Z; SABO, E; MISSELEVITCH, I et al.American journal of medical genetics. 1998, Vol 76, Num 3, pp 238-244, issn 0148-7299Article

Early prenatal diagnosis of polycystic pancreas with narrow thorax and short limb dwarfismBRONSTEIN, M; REICHLER, A; BOROCHOWITZ, Z et al.American journal of medical genetics. 1994, Vol 49, Num 1, pp 6-9, issn 0148-7299Article

Achondrogenesis II-Hypochondrogenesis: variability versus heterogeneityBOROCHOWITZ, Z; ORNOY, A; LACHMAN, R et al.American journal of medical genetics. 1986, Vol 24, Num 2, pp 273-288, issn 0148-7299Article

New multiple congenital anomalies : mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvementBOROCHOWITZ, Z; PAVONE, L; MAZOR, G et al.American journal of medical genetics. 1992, Vol 43, Num 4, pp 678-685, issn 0148-7299Article

Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type : a congenital familial skeletal dysplasia with distinctive features and histopathologyBOROCHOWITZ, Z; LANGER, L. O; GRUBER, H. E et al.American journal of medical genetics. 1993, Vol 45, Num 3, pp 320-326, issn 0148-7299Article

Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosisFALIK-ZACCAI, T. C; ZEIGLER, M; BARGAL, R et al.Prenatal diagnosis. 2003, Vol 23, Num 3, pp 211-214, issn 0197-3851, 4 p.Article

DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)FALIK-BORENSTEIN, T. C; HOLMES, S. A; BOROCHOWITZ, Z et al.Prenatal diagnosis. 1995, Vol 15, Num 4, pp 345-349, issn 0197-3851Article

Predisposition to the fragile X syndrome in jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypeFALIK-ZACCAI, T. C; SHACHAK, E; YALON, M et al.American journal of human genetics. 1997, Vol 60, Num 1, pp 103-112, issn 0002-9297Article

Interstitial deletion (6)q13q15GERSHONI-BARUCH, R; MANDEL, H; BAR EL, H et al.American journal of medical genetics. 1996, Vol 62, Num 4, pp 345-347, issn 0148-7299Article

Ataxia-telangiectasia : linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeZIV, Y; FRYDMAN, M; BOROCHOWITZ, Z et al.Human genetics. 1992, Vol 88, Num 6, pp 619-626, issn 0340-6717Article

Very low maternal serum unconjugated estriol and prenatal diagnosis of steroid sulfatase deficiencyDAVID, M; ISRAEL, N; MERKSAMER, R et al.Fetal diagnosis and therapy. 1995, Vol 10, Num 2, pp 76-80, issn 1015-3837Article