AUTOSOMAL DOMINANT ANIRIDIA IN ASSOCIATION WITH CRANIOPHARYNGIOMABLETHEN SL; TAYSI K.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 6; PP. 575-576; BIBL. 7 REF.Article

CONCORDANT CONGENITAL MALFORMATIONS IN TWINS WITH INHERITED TRANSLOCATION: T(9P-;13Q+)SEKHON GS; TAYSI K.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 271-276; BIBL. 4 REF.Article

PARTIAL TRISOMY OF CHROMOSOME NO 1 IN TWO ADULT BROTHERS DUE TO MATERNAL TRANSLOCATION (1Q-;6P+)TAYSI K; SEKHON GS.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 3; PP. 277-285; BIBL. 9 REF.Article

TRISOMY D AND THE CYCLOPS MALFORMATION = TRISOMIED ET CYCLOPIETAYSI K; TINAZTEPE K.1972; AMER. J. DIS. CHILD.; U.S.A.; DA. 1972; VOL. 124; NO 5; PP. 710-713; BIBL. 23REF.Serial Issue

A NEW SYNDROME OF PROXIMAL DELETION OF THE LONG ARM OF CHROMOSOME 1:1Q21-23->1Q25TAYSI K; SEKHON GS; HILLMAN RE et al.1982; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 4; PP. 423-430; BIBL. 10 REF.Article

FAMILIAL WILLIAMS SYNDROMECORTADA X; TAYSI K; HARTMANN AF et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 3; PP. 173-176; BIBL. 8 REF.Article

PARTIAL TRISOMY 15 AND INTRACTABLE SEIZURESTAYSI K; DEVIVO DC; SEKHON GS et al.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 3; PP. 445-447Article

FAMILIAL PERICENTRIC INVERSION 19JORDAN DK; TAYSI K; BLACKWELL NL et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 3; PP. 222-225; BIBL. 9 REF.Article

TERMINAL LONG ARM DELETION OF CHROMOSOME 7 AND RETINOCHOROIDAL COLOBOMATAYSI K; BURDE RM; ROHRBAUGH JR et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 3; PP. 159-161; ABS. FRE; BIBL. 10 REF.Article

PRESUMPTIVE LONG ARM DELETION OF CHROMOSOME 8: A NEW SYNDROME.TAYSI K; NOETZEL MJ; STRAUSS AW et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 49-53; BIBL. 3 REF.Article

A TERMINAL LONG ARM DELETION OF CHROMOSOME 16 IN A DYSMORPHIC INFANT: 46, XY, DEL (16) (Q22)TAYSI K; FISHMAN M; SEKHON GS et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 343-347; BIBL. 4 REF.Article

PARTIAL TRISOMY 13 AS A RESULT OF DE NOVO (6 P; 13 Q) TRANSLOCATIONJONES LA; TAYSI K; STRAUSS AW et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 245-249; BIBL. 6 REF.Article

DOWN'S SYNDROME PHENOTYPE AND AUTOSOMAL GENE INACTIVATION IN A CHILD WITH PRESUMED (X;21) DE NOVO TRANSLOCATIONTAYSI K; SPARKES RS; O'BRIEN TJ et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 144-148; BIBL. 15 REF.Article

TRISOMY 2S IN BONE MARROW CELLS OF A PATIENT WITH A PROLONGED PRELEUKEMIC PHASESIKAND GS; TAYSI K; STRANDJORD SE et al.1980; MED. PEDIATR. ONCOL.; ISSN 0098-1532; USA; DA. 1980; VOL. 8; NO 3; PP. 237-242; BIBL. 11 REF.Article

PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 5: A CASE DUE TO BALANCED PATERNAL TRANSLOCATION AND REVIEW OF THE LITERATUREJONES LA; JORDAN DK; TAYSI K et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 37-42; BIBL. 4 REF.Article

A GIANT SHORT ARM OF NO. 21 CHROMOSOME IN MOTHER OF 21/21 TRANSLOCATION MONGOL.TUNCBILEK E; BOBROW M; CLARKE G et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 5; PP. 411-412; BIBL. 6 REF.Article

HYPERPHALANGY AND CLINODACTYLY OF THE INDEX FINGER WITH PIERRE ROBIN ANOMALY: CATEL-MANZKE SYNDROME: A CASE REPORT AND REVIEW OF THE LITERATURESUNDARAM V; TAYSI K; HARTMANN AF JR et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 6; PP. 407-410; BIBL. 7 REF.Article

DUPLICATION-DEFICIENCY PRODUCT OF A PERICENTRIC INVERSION IN MAN: A CAUSE OF D₁ TRISOMY SYNDROME = DUPLICATION-DEFICIT RESULTANT D'UNE INVERSION PERICENTRIQUE CHEZ L'HOMME: UNE CAUSE DU SYNDROME DE TRISOMIED₁TAYSI K; BOBROW M; BALCI S et al.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 2; PP. 263-268; BIBL. 10REF.Serial Issue

Brief clinical report: congenital absence of left pericardium in a familyTAYSI, K; HARTMANN, A. F; SHACKELFORD, G. D et al.American journal of medical genetics. 1985, Vol 21, Num 1, pp 77-83, issn 0148-7299Article

Trisomy 6q22→6qter due to maternal 6;21 translocation: case report and review of the literatureTAYSI, K; CHAO, W. T; MONAGHAN, N et al.Annales de génétique (Paris). 1983, Vol 26, Num 4, pp 243-246, issn 0003-3995Article

Comprehensive ultrasound examination in a private perinatal practiceOTT, W. J; ARIAS, F; SHELDON, G et al.American journal of perinatology. 1995, Vol 12, Num 6, pp 385-391, issn 0735-1631Article

18q Deletion syndrome in a child with steroid-17,20-lyase deficiencyCHASALOW, F. I; BLETHEN, S. L; KNIGHT, S. M et al.Steroids. 1986, Vol 47, Num 6, pp 421-429, issn 0039-128XArticle

Ring chromosome 6: variability in phenotypic expressionPEEDEN, J. N; SCARBROUGH, P; TAYSI, K et al.American journal of medical genetics. 1983, Vol 16, Num 4, pp 563-573, issn 0148-7299Article