GENETICS OF AFFECTIVE DISORDERS. I. FAMILIAL INCIDENCE STUDY OF BIPOLAR, UNIPOLAR AND SCHIZO-AFFECTIVE ILLNESSES.SUSLAK L; SHOPSIN B; SILBEY E et al.1976; NEUROPSYCHOBIOLOGY; SWITZ.; DA. 1976; VOL. 2; NO 1; PP. 18-27; BIBL. 17 REF.Article

GENETICS OF AFFECTIVE DISORDERS. II. MORBIDITY RISK AND GENETIC TRANSMISSION.SHOPSIN B; MENDLEWICZ J; SUSLAK L et al.1976; NEUROPSYCHOBIOLOGY; SWITZ.; DA. 1976; VOL. 2; NO 1; PP. 28-36; BIBL. 24 REF.Article

Transmitting balanced translocation carrier information within families: a follow-up studySUSLAK, L; PRICE, D. M; DESPOSITO, F et al.American journal of medical genetics. 1985, Vol 20, Num 2, pp 227-232, issn 0148-7299Article

Monozygosity and holoprosencephaly: cleavage disorders of the midline fieldSUSLAK, L; MIMMS, G. M; DESPOSITO, F et al.American journal of medical genetics. 1987, Vol 28, Num 1, pp 99-102, issn 0148-7299Article

DWARFISM ASSOCIATED WITH PRENATAL VENTRICULOMEGALYSHIH LY; FILKINS K; SUSLAK L et al.1983; PRENATAL DIAGNOSIS; ISSN 0197-3851; GBR; DA. 1983; VOL. 3; NO 1; PP. 69-73; BIBL. 9 REF.Article

Uniparental disomy explains the occurrence of the Angelman of Prader-Willi syndrome in patients with an additional small inv dup(15) chromosomeROBINSON, W. P; WAGSTAFF, J; BERNASCONI, F et al.Journal of medical genetics. 1993, Vol 30, Num 9, pp 756-760, issn 0022-2593Article

Crouzon syndrome with periapical cemental dysplasia and acanthosis nigricans: the pleiotropic effect of a single gene?SUSLAK, L; GLISTA, B; GERTZMAN, G. B et al.Birth defects original article series. 1985, Vol 21, Num 2, pp 127-134, issn 0547-6844Article

Interstitial insertion of Y-specific DNA sequences including SRY into chromosome 4 in a 45,X male childYENAMANDRA, A; DEANGELO, P; AVIV, H et al.American journal of medical genetics. 1997, Vol 72, Num 2, pp 125-128, issn 0148-7299Article

Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicismCHRISTIAN, S. L; SMITH, A. C. M; LEDBETTER, D. H et al.Prenatal diagnosis. 1996, Vol 16, Num 4, pp 323-332, issn 0197-3851Article

Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophyBRUZUSTOWICZ, L. M; ALLITTO, B. A; GILLIAM, T. C et al.American journal of human genetics. 1994, Vol 54, Num 3, pp 482-488, issn 0002-9297Article

Courzon syndrome : prenatal ultrasound diagnosis by binocular diametersLEO, M. V; SUSLAK, L; GANESH, V. L et al.Obstetrics and gynecology (New York. 1953). 1991, Vol 78, Num 5, pp 906-908, issn 0029-7844, 2Article

Crouzon syndrome with periapical cemental dysplasia and acanthosis nigricans: the pleiotropic effect of a single gene?SUSLAK, L; GLISTA, B; GERTZMAN, G. B et al.Birth defects original article series. 1985, Vol 21, Num 2, pp 127-134, issn 0547-6844Article

Brief clinical report: gene dosage studies supporting localization of the structural gene for galactose-1-phosphate uridyl transferase (GALT) to band p13 of chromosome 9LING YU SHIH; SUSLAK, L; ROSIN, I et al.American journal of medical genetics. 1984, Vol 19, Num 3, pp 539-543, issn 0148-7299Article