STUDIES OF BANDE CHROMOSOMES IN PATIENTS WITH ACUTE LYMPHOCYTIC LEUKEMIA, INCLUDING ONE PATIENT WITH THE BURKITT-TYPE (L₃)SHABTAI F; HALBRECHT I.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 1; PP. 11-18; BIBL. 29 REF.Article

INTERPRETATION OF A MARKER CHROMOSOME 17P IN MULTIPLE MYELOMASHABTAI F; HALBRECHT I.1981; HEREDITAS; ISSN 0018-0661; SWE; DA. 1981; VOL. 95; NO 1; PP. 11-14; BIBL. 14 REF.Article

RISK OF MALIGNANCY AND CHROMOSOMAL POLYMORPHISM: A POSSIBLE MECHANISM OF ASSOCIATIONSHABTAI F; HALBRECHT I.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 1; PP. 73-77; BIBL. 25 REF.Article

THE FRAGILE SITE ON CHROMOSOME 16 (Q21Q22): DATA ON FOUR NEW FAMILIESSHABTAI F; BICHACHO S; HALBRECHT I et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 19-22; BIBL. 14 REF.Article

PRIMARY AMENORRHEA WITH A NEW MOSAIC 46, XXQI/47, XXQI XP^-. CONSIDERATION ON THE X ISOCHROMOSOME FORMATION AND X CHROMOSOME INACTIVATION.HALBRECHT I; SHABTAI F; KUPFERSTAIN C et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 1; PP. 63-69; ABS. ITAL. FR. ALLEM.; BIBL. 20 REF.Article

CHROMOSOME 17 HAS A REAL FRAGILE SITE AT P12SHABTAI F; KLAR D; HALBRECHT I et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 2; PP. 177-179; BIBL. 6 REF.Article

CYTOGENIC OBSERVATIONS IN INFERTILE MEN WORKING WITH INSECTICIDAL COMPOUNDSSHABTAI F; BICHACHO S; HALBRECHT I et al.1978; ACTA CG GENET. MED. GEMELLOL.; ITA; DA. 1978; VOL. 27; PP. 51-56; BIBL. 24 REF.Article

TRIPLE MOSAICISM WITH TWO AUTOSOMALLY UNBALANCED CELL LINES IN A PHENOTYPICALLY NORMAL OLIGOSPERMIC MAN.SHABTAI F; BICHACHO S; HALBRECHT I et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 2; PP. 177-180; BIBL. 15 REF.Article

PURE TRISOMY 17P IN 60% OF CELLSSHABTAI F; SHALEV A; CHEMKE J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 3; PP. 263-268; BIBL. 12 REF.Article

LEBER'S OPTIC NEUROPATHY: A CYTOGENETIC STUDY OF A FAMILYAVISAR R; SHABTAI F; HALBRECHT I et al.1980; J. PEDIATR. OPHTHALMOL. STRABISMUS; ISSN 0191-3913; USA; DA. 1980; VOL. 17; NO 4; PP. 229-231; BIBL. 8 REF.Article

FAMILIAL FRAGILITY ON CHROMOSOME 16 (FRA 16Q22) ENHANCED BY BOTH INTERFERON AND DISTAMYCIN ASHABTAI F; KLAR D; BICHACHO S et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 4; PP. 341-344; BIBL. 23 REF.Article

NEW COMPLEX PH' TRANSLOCATION T(10; 14; 22) IN BONE MARROW CELLS AND IN PHA-STIMULATED PERIPHERAL BLOOD CULTURES IN CHRONIC MYELOCYTIC LEUKAEMIASHABTAI F; GAFTER U; WEISS S et al.1980; J. CANCER RES. CLIN. ONCOL.; DEU; DA. 1980; VOL. 96; NO 3; PP. 287-294; BIBL. 2 P.Article

ULTRASTRUCTURAL AND CHROMOSOMAL STUDIES IN A PATIENT WITH HYPERGRANULAR (M₃) PROMYELOCYTIC LEUKEMIA WITH TWO ABNORMAL CLONESZAHAVI I; SHABTAI F; APPEL S et al.1982; ACTA HAEMATOLOGICA; ISSN 0001-5792; CHE; DA. 1982; VOL. 68; NO 1; PP. 52-57; BIBL. 17 REF.Article

49,XYYYY. A CASE REPORTSIROTA L; ZLOTOGORA Y; SHABTAI F et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 2; PP. 87-93; BIBL. 11 REF.Article

TWO ABNORMAL CLONES IN THE BONE MARROW CELLS OF A PATIENT WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIACOHEN AM; SHABTAI F; LEWINSKI V et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 3; PP. 178-182; BIBL. 23 REF.Article

MARKER CHROMOSOMES IN A FAMILY WITH HIGH INCIDENCE OF CANCER = MARQUEURS CHROMOSOMIQUES CHEZ UNE FAMILLE AYANT UNE FREQUENCE ELEVEE DE CANCERSSHABTAI F; KLAR D; SCHWARTZ A et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 9; NO 3; PP. 281-287; ABS. ENG; BIBL. 17 REF.; FIGArticle

TRIPLE MOSAICISM 45,XY,-18/46, XY/47, XY,+18FRYDMAN M; SHABTAI F; BARAK Y et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 3; PP. 232-234; BIBL. 13 REF.Article

TRANSMISSION AND SCANNING ELECTRON MICROSCOPY STUDY ON PLASMA CELL LEUKEMIA.KLEIN B; LEWINSKI U; SHABTAI F et al.1977; BLUT; DTSCH.; DA. 1977; VOL. 35; NO 1; PP. 11-19; ABS. ALLEM.; BIBL. 15 REF.Article

APLASTIC ANEMIA FOLLOWED BY LEUKEMIA IN CONGENITAL TRISOMY 8 MOSAICISM. ULTRASTRUCTURAL STUDIES OF POLYMORPHONUCLEAR CELLS IN PERIPHERAL BLOODGAFTER U; SHABTAI F; KAHN Y et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 2; PP. 134-142; BIBL. 30 REF.Article

NORMAL PSYCHOMOTOR DEVELOPMENT IN A CHILD WITH MOSAIC TRISOMY AND PERICENTRIC INVERSION OF CHROMOSOME 9FRYDMAN M; SHABTAI F; HALBRECHT I et al.1981; J. MET. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 390-392; BIBL. 15 REF.Article

A NEW FAMILY WITH A SATELLITED YSHABTAI F; EILAM N; ELIAN E et al.1981; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1981; VOL. 24; NO 4; PP. 223-225; ABS. FRE; BIBL. 18 REF.Article

A NEW CYTOGENETIC ASPECT OF POLYCYTHEMIA VERA.SHABTAI F; WEISS S; VAN DER LIJN E et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 281-287; BIBL. 21 REF.Article

Fibrous dysplasia and cherubism as an hereditary familial disease: follow-up of four generationsZOHAR, Y; GRAUSBORD, R; SHABTAI, F et al.Journal of cranio-maxillo-facial surgery. 1989, Vol 8, Num 17, pp 340-344, issn 1010-5182Article

Interstitial 7q deletion [46,XY,del(7)(pter→cen::q112→qter)] in a retarded quadriplegic boy with normal beta glucuronidaseFRYDMAN, M; STEINBERGER, J; SHABTAI, F et al.American journal of medical genetics. 1986, Vol 25, Num 2, pp 245-249, issn 0148-7299Article

PH¹-POSITIVE ACUTE LYMPHOCYTIC LEUKEMIA WITH CHROMOSOME 7 ABNORMALITIES.MANDEL EM; SHABTAI F; GAFTER U et al.1977; BLOOD; U.S.A.; DA. 1977; VOL. 49; NO 2; PP. 281-287; BIBL. 1 P.Article