Works matching IS 00099163 AND DT 1984 AND VI 26 AND IP 6

Results: 15

Abnormal chromosome in Prader-Willi syndrome.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 597, doi. 10.1111/j.1399-0004.1984.tb01110.x

By:

Goh, Kong-oo;
Herrmann, Marie A.;
Campbell, Robert G.;
Thompson, Dean

Publication type:

Article

Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 579, doi. 10.1111/j.1399-0004.1984.tb01107.x

By:

Poulos, A.;
Sharp, P.;
Whiting, M.

Publication type:

Article

Fetal mortality in sibships of cases with neural tube defects.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 563, doi. 10.1111/j.1399-0004.1984.tb01104.x

By:

Lippman, Abby

Publication type:

Article

Mechanisms that cause Craniofacial and Oral Birth Defects.

Published in:: Clinical Genetics, 1984, v. 26, n. 6, p. 608, doi. 10.1111/j.1399-0004.1984.tb01113.x
Publication type:: Article

Interstitial deletion of the long arm of chromosome 6 [del(6)(q16q22)]: case report and review of the literature.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 574, doi. 10.1111/j.1399-0004.1984.tb01106.x

By:

Schwartz, M. F.;
Kaffe, S.;
Wallace, S.;
Desnick, R. J.

Publication type:

Article

Isochromosome 18q with karyotype 46, XX, i(18q). Cytogenetics and pathology.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 549, doi. 10.1111/j.1399-0004.1984.tb01102.x

By:

Froster-Iskenius, Ursula;
Coerdt, Wiltrud;
Rehder, Helga;
Schwinger, E.

Publication type:

Article

The fragile X syndrome: A study of 83 families.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 497, doi. 10.1111/j.1399-0004.1984.tb01099.x

By:

Fryns, J. P.

Publication type:

Article

Two fertile Turner women in a family.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 591, doi. 10.1111/j.1399-0004.1984.tb01109.x

By:

Ayuso, Ma Carmen;
Bello, Ma José;
Benitez, Javier;
Sanchez-Cascos, Andrés;
Mendoza, Gladys

Publication type:

Article

Familial occurrence of azoospermia and extreme oligozoospermia.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 555, doi. 10.1111/j.1399-0004.1984.tb01103.x

By:

Budde, Willem J. A. M.;
Verjaal, Marianne;
Hamerlynck, Johan V. Th. H.;
Bobrow, Martin

Publication type:

Article

Cytogenetics of Prader-Willi Syndrome.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 602, doi. 10.1111/j.1399-0004.1984.tb01111.x

By:

Hoo, J. J.

Publication type:

Article

Reply to Dr. Hoo.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 606, doi. 10.1111/j.1399-0004.1984.tb01112.x

By:

Köhler, Angelika

Publication type:

Article

Epinephrine-induced platelet aggregation. A twin study.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 543, doi. 10.1111/j.1399-0004.1984.tb01101.x

By:

Gaxiola, Blanca;
Friedl, Waltraut;
Propping, Peter

Publication type:

Article

Weyers acrodental dysostosis in a family.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 587, doi. 10.1111/j.1399-0004.1984.tb01108.x

By:

Roubicek, Martin;
Spranger, Jurgen

Publication type:

Article

Measuring the genetic contribution of a single locus to a multilocus disease.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 529, doi. 10.1111/j.1399-0004.1984.tb01100.x

By:

Rotter, Jerome I.;
Landaw, Elliot M.

Publication type:

Article

New anomalies found in the 11q- syndrome.

Published in:

Clinical Genetics, 1984, v. 26, n. 6, p. 569, doi. 10.1111/j.1399-0004.1984.tb01105.x

By:

Sirota, L.;
Shabtai, F.;
Landman, I.;
Halbrecht, I.;
Dulitzky, F.

Publication type:

Article