K. Taysi

发表

A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22).

K. Taysi, M. Fishman, G. Sekhon, 1978, Birth defects original article series.

Autosomal dominant aniridia in association with craniopharyngioma.

K. Taysi, S. Blethen, 1981, American journal of diseases of children.

Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel‐Manzke syndrome. A case report and review of the literature

J. Keating, G. Shackelford, K. Taysi, 1982, Clinical genetics.

Trisomy 21 in bone marrow cells of a patient with a prolonged preleukemic phase.

T. Vietti, K. Taysi, R. Griffith, 1980, Medical and pediatric oncology.

Mosaic mongolism. II. Cytogenic studies.

K. Taysi, G. Kohn, W. Mellman, 1970, The Journal of pediatrics.

Mosaic mongolism. I. Clinical correlations.

K. Taysi, G. Kohn, W. Mellman, 1970, The Journal of pediatrics.

Obstetric ultrasonographic findings and fetal chromosomal abnormalities: refining the association.

W. Ott, K. Taysi, 2001, American journal of obstetrics and gynecology.

CD30+ anaplastic large‐cell lymphoma with aberrant expression of CD13: Case report and review of the literature

C. Dunphy, J. Manes, K. Taysi, 2000, Journal of clinical laboratory analysis.

Possible abnormalities of steroid secretion in children with Smith-Lemli-Opitz syndrome and their parents

K. Taysi, S. Blethen, F. Chasalow, 1985, Steroids.

A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongol.

M. Bobrow, K. Taysi, G. Clarke, 1976, Journal of medical genetics.

THE CAT‐EYE SYNDROME WITH UNUSUAL SKELETAL MALFORMATIONS

S. Balcı, K. Taysi, B. Say, 1974, Acta Paediatrica Scandinavica.

Satellite association: Giemsa banding studies in parents of Down's syndrome patients *

K. Taysi, 1975, Clinical genetics.

Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q-;6p+)

K. Taysi, G. Sekhon, 1978, Human Genetics.

Presumptive long arm deletion of chromosome 8: a new syndrome?

A. Strauss, K. Taysi, M. Noetzel, 1979, Human Genetics.

OCULODENTODIGITAL DYSPLASIA SYNDROME

K. Taysi, B. Say, G. Gürsu, 1971, Acta paediatrica Scandinavica.

Partial duplication of the long arm of chromosome 5: A case due to balanced paternal translocation and review of the literature

A. Strauss, K. Taysi, D. K. Jordan, 1979, Human Genetics.

Partial trisomy for the short arm of chromosome 2 due to familial balanced translocation

K. Taysi, G. Sekhon, Richard Rath, 1978, Human Genetics.

Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.

A. Strauss, K. Taysi, C. Padmalatha, 1982, Annales de genetique.

Partial trisomy 10q in three unrelated patients.

K. Taysi, N. Beraha, V. Yang, 1983, Annales de genetique.

Ring chromosome 6: variability in phenotypic expression.

F. Luthardt, K. Taysi, J. Peeden, 1983, American journal of medical genetics.

Partial trisomy of the short arm of chromosome 8 resulting from balanced maternal translocation.

G. Shackelford, K. Taysi, A. Hartmann, 1980, Journal of medical genetics.

Congenital absence of left pericardium in a family.

G. Shackelford, K. Taysi, V. Sundaram, 1985, American journal of medical genetics.

Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation.

R. Sparkes, K. Taysi, T. O'Brien, 1982, Journal of medical genetics.

Familial Williams Syndrome

K. Taysi, E. Mallinckrodt, A. Hartmann, 1980, Clinical genetics.

Limitations of metachromasia as a diagnostic aid in pediatrics.

K. Taysi, H. Punnett, M. Kistenmacher, 1969, The New England journal of medicine.

A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21–23→1q25

J. Opitz, R. Hillman, K. Taysi, 1982 .

A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.

R. Hillman, K. Taysi, G. Sekhon, 1982, American journal of medical genetics.

18q Deletion syndrome in a child with steroid-17,20-lyase deficiency

K. Taysi, S. Blethen, F. Chasalow, 1986, Steroids.

Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome.

M. Bobrow, S. Balcı, K. Taysi, 1973, The Journal of pediatrics.

Duplication~deficiency product of a pericentric inversion in man: A cause of 191 trisomy

M. Bobrow, S. Balcı, K. Taysi, 1973 .

Interstitial deletion of the long arm of chromosome 2: case report and review of literature.

K. Taysi, J. R. Heersma, L. A. Jones, 1981, Annales de genetique.

Partial trisomy of short arm of chromosome 6: a case due to paternal balanced translocation.

K. Taysi, C. G. Henry, M. Yüksel, 1980, The Turkish journal of pediatrics.

Familial pericentric inversion 19.

K. Taysi, D. K. Jordan, N. L. Blackwell, 1980, Journal of medical genetics.

Preconceptional counseling.

K. Taysi, 1988, Obstetrics and gynecology clinics of North America.

Aarskog's syndrome with Hirschsprung's disease, midgut malrotation, and dental anomalies.

J. Mulvihill, G. Shackelford, K. Taysi, 1980, Journal of medical genetics.

PARTIAL TRISOMY 15 AND INTRACTABLE SEIZURES

D. Devivo, K. Taysi, G. Sekhon, 1979, Acta Paediatrica Scandinavica.

Terminal long arm deletion of chromosome 7 and retino-choroidal coloboma.

R. Burde, K. Taysi, J. Rohrbaugh, 1982, Annales de Genetique.

Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.

K. Taysi, 1983, American journal of medical genetics.

Partial trisomy 11p with interatrial septal aneurysm. Case report and literature review.

K. Taysi, K. Aleck, C. Mongkolsmai, 1985, Annales de Genetique.

Familial pericentric inversion 19.

K. Taysi, D. K. Jordan, Nora L BLACKWELLt, 1980, Journal of medical genetics.

Partial trisomy 13 as a result of de novo (6p;13q) translocation

A. Strauss, K. Taysi, A. Hartmann, 1979, Human Genetics.

Immunological studies in ataxia‐telangiectasia

K. Taysi, B. Say, K. Yalaz, 1974, Clinical genetics.