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PARTIAL DELETION OF LONG ARM OF CHROMOSOME 11: DEL(11) (Q23).KAFFE S; HSU YF; SACHDEV RK et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 6; PP. 323-328; BIBL. 14 REF.Article

PRENATAL DIAGNOSIS OF BILATERAL RENAL AGENESIS.KAFFE S; GODMILOW L; WALKER BA et al.1977; OBSTETR. AND GYNECOL.; U.S.A.; DA. 1977; VOL. 49; NO 4; PP. 478-480; BIBL. 15 REF.Article

SUPERNUMERARY SMALL RING CHROMOSOME.KAFFE S; KIM HJ; HSU LYF et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 6; PP. 447-450; BIBL. 19 REF.Article

GALACTOSEMIA. REPOSITORY IDENTIFICATION NOS. GM-438 TO GM-442.KAFFE S; BERATIS NG; HIRSCHHORN K et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 1; PP. 62-64; BIBL. 3 REF.Article

ASSOCIATION OF 59- AND REFRACTORY ANEMIAKAFFE S; HSU LYF; HOFFMAN R et al.1978; AMER. J. HEMATOL.; USA; DA. 1978; VOL. 4; NO 3; PP. 269-272; BIBL. 10 REF.Article

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A heterozygous defect for structurally altered pro-α2 chain of type I procollagen in a mild variant of osteogenesis imperfecta: the altered structure decreases the thermal stability of procollagen and makes it resistant to procollagen N-proteinaseSIPPOLA, M; KAFFE, S; PROCKOP, D. J et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 22, pp 14094-14100, issn 0021-9258Article

VARIABLE CELL-MEDIATED IMMUNE DEFECTS IN A FAMILY WITH CANDIDA ENDOCRINOPATHY SYNDROME = DEFICIENCES VARIABLES D'IMMUNITE A MEDIATION CELLULAIRE DANS UNE FAMILLE PRESENTANT LE SYNDROME D'ENDOCRINOPATHIE A CANDIDAKAFFE S; PETIGROW CS; CAHILL LT et al.1975; CLIN. EXPER. IMMUNOL.; G.B.; DA. 1975; VOL. 20; NO 3; PP. 397-408; BIBL. 1P.1/2Article

Amniotic fluid alpha-fetoprotein levels and prenatal diagnosis of autosomal trisomiesKAFFE, S; PERLIS, T. E; HSU, L. Y. F et al.Prenatal diagnosis. 1988, Vol 8, Num 3, pp 183-187, issn 0197-3851Article

Unilateral microscopic gonadoblastoma in a prepubertal Turner mosaic with Y chromosome material identified by restriction fragment analysisSHAH, K. D; KAFFE, S; GILBERT, F et al.American journal of clinical pathology. 1988, Vol 90, Num 5, pp 622-627, issn 0002-9173Article

Paternal uniparental disomy for chromosome 14 : A case report and reviewCOTTER, P. D; KAFFE, S; MCCURDY, L. D et al.American journal of medical genetics. 1997, Vol 70, Num 1, pp 74-79, issn 0148-7299Article

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNADEPINET, T. W; ZACKOWSKI, J. L; ZINN, A. B et al.Human molecular genetics (Print). 1997, Vol 6, Num 8, pp 1195-1204, issn 0964-6906Article