Works matching IS 00099163 AND DT 1981 AND VI 20 AND IP 3

Results: 15

Dermatoglyphic and cytogenetic studies in parents of children with trisomy 21.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 203, doi. 10.1111/j.1399-0004.1981.tb01830.x

By:

Schmidt, Rina;
Dar, Hanna;
Nitowsky, Harold M.

Publication type:

Article

Recurrent unilateral hand malformations in siblings.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 225, doi. 10.1111/j.1399-0004.1981.tb01834.x

By:

Hecht, Jacqueline T.;
Scott, Charles I.

Publication type:

Article

Pericentric X chromosome in a family.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 234, doi. 10.1111/j.1399-0004.1981.tb01836.x

By:

Soler, Anna;
Salami, Carme;
Balmes, Isabel;
Carrio, Anna;
Tejada, Isabel;
Farguell, Teresa;
Cols, Neus;
Cararach, Josep;
Fortuny, Albert

Publication type:

Article

Hyperglycinemia and pregnancy.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 238, doi. 10.1111/j.1399-0004.1981.tb01839.x

By:

Coulam, Carolyn B.

Publication type:

Article

Histidinaemia in Sweden.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 229, doi. 10.1111/j.1399-0004.1981.tb01835.x

By:

Aim, J.;
Holmgren, G.;
Larsson, A.;
Schimpfessel, L.

Publication type:

Article

High resolution protein mapping in fibroblast cell lines and hair roots from patients with genetic disease.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 217, doi. 10.1111/j.1399-0004.1981.tb01832.x

By:

WILLERS, I.;
SINGH, S.;
GOEDDE, H. W.;
KLOSE, J.

Publication type:

Article

March of Dimes medical symposium: Fetal Hypoxia and Brain Damage.

Published in:: Clinical Genetics, 1981, v. 20, n. 3, p. 241, doi. 10.1111/j.1399-0004.1981.tb01841.x
Publication type:: Article

Mannosidosis: two brothers with different degrees of disease severity.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 191, doi. 10.1111/j.1399-0004.1981.tb01829.x

By:

Mitchell, Mark L.;
Erickson, Robert P.;
Schmid, Douglas;
Hieber, Virginia;
Poznanski, Andrew K.;
Hicks, Samuel P.

Publication type:

Article

The genetics of omphalocele.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 236, doi. 10.1111/j.1399-0004.1981.tb01837.x

By:

Adeyokunnu, A. A.

Publication type:

Article

Partial chromosome 4 trisomy.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 179, doi. 10.1111/j.1399-0004.1981.tb01827.x

By:

Qazi, Qutub H.;
Madahar, Cecily;
Kanchanapoomi, R.;
Price, Winston;
Chua, Albina;
Beller, Eva

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1981, v. 20, n. 3, p. 240, doi. 10.1111/j.1399-0004.1981.tb01840.x
Publication type:: Article

Familial fibromatosis.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 211, doi. 10.1111/j.1399-0004.1981.tb01831.x

By:

Young, I. D.;
Fortt, R. W.

Publication type:

Article

Third case of a distinct variant of the Ehlers-Danlos Syndrome (EDS).

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 222, doi. 10.1111/j.1399-0004.1981.tb01833.x

By:

Hernández, A.;
Aguirre-Negrete, M. G.;
Liparoli, J. C.;
Cantú, J. M.

Publication type:

Article

Klinefelter syndrome and the Xq.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 237, doi. 10.1111/j.1399-0004.1981.tb01838.x

By:

Fryns, J. P.

Publication type:

Article

Prenatal diagnosis of Fanconi anemia.

Published in:

Clinical Genetics, 1981, v. 20, n. 3, p. 185, doi. 10.1111/j.1399-0004.1981.tb01828.x

By:

Voss, R.;
Kohn, G.;
Shaham, M.;
BENZUR, Z.;
Arnon, J.;
Ornoy, A.;
Yaffe, H.;
Golbus, M.;
Auerbach, A. D.

Publication type:

Article