Works matching IS 00099163 AND DT 1977 AND VI 11 AND IP 1

Results: 15

Sclerosteosis - An autosomal recessive disorder.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 1, doi. 10.1111/j.1399-0004.1977.tb01269.x

By:

Beighton, Peter;
Davidson, James;
Durr, Lecia;
Hamersma, Herman

Publication type:

Article

Sex-linked chondrodysplasia punctata?

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 73, doi. 10.1111/j.1399-0004.1977.tb01281.x

By:

Happle, K.;
Matthiass, H.-H.;
Macher, E.

Publication type:

Article

Partial Trisomy 17.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 77, doi. 10.1111/j.1399-0004.1977.tb01282.x

By:

Biederman, Brian

Publication type:

Article

Serum pancreatic isoamylases in the diagnosis of cystic fibrosis heterozygotes: A non-valuable test.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 43, doi. 10.1111/j.1399-0004.1977.tb01276.x

By:

Schiøtz, P. O.;
Magid, E.

Publication type:

Article

Selective hypoaldosteronism in Iranian Jews: An autosomal recessive trait.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 25, doi. 10.1111/j.1399-0004.1977.tb01273.x

By:

Cohen, Tirza;
Theodor, Rachel;
Rösler, Ariel

Publication type:

Article

Amniocentesis in prenatal diagnosis A controlled series of 78 cases.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 18, doi. 10.1111/j.1399-0004.1977.tb01272.x

By:

Munk-Andersen, Ebbe;
Weber, Jan;
Mikkelsen, Margareta

Publication type:

Article

A chromosome No. 2 abnormality in a child with a few congenital defects.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 8, doi. 10.1111/j.1399-0004.1977.tb01270.x

By:

Escobar, Javier I.;
Lakatua, David J.;
Streifel, Barbara;
Virnig, Norman L.;
Sanchez, Otto

Publication type:

Article

A new estimate of the achondroplasia mutation rate.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 31, doi. 10.1111/j.1399-0004.1977.tb01274.x

By:

Gardner, R. J. M.

Publication type:

Article

Universal permanent alopecia, psychomotor epilepsy, pyorrhea and mental subnormality.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 13, doi. 10.1111/j.1399-0004.1977.tb01271.x

By:

Shokeir, M. H. K.

Publication type:

Article

Infantile polymyoclonus: Its occurrence in second cousins.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 53, doi. 10.1111/j.1399-0004.1977.tb01278.x

By:

Robinson, Geoffrey C.;
Jan, James E.;
Dunn, Henry G.

Publication type:

Article

Translocation 9q/13q resulting in duplication (trisomy 9pter→9q22) and deficiency (monosomy 13pter→13q12).

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 46, doi. 10.1111/j.1399-0004.1977.tb01277.x

By:

Howard-Peebles, Patricia N.;
Yarbrough, Karen M.;
Stoddard, Gayle R.;
Rary, Jack M.

Publication type:

Article

Linkage studies on the Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 57, doi. 10.1111/j.1399-0004.1977.tb01279.x

By:

Skre, H.;
Berg, K.

Publication type:

Article

Partial 7q trisomy.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 39, doi. 10.1111/j.1399-0004.1977.tb01275.x

By:

Berger, R.;
Turc, C.;
Wachter, H.;
Begue, G.

Publication type:

Article

Trisomy 9p syndrome and XYY syndrome in siblings.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 67, doi. 10.1111/j.1399-0004.1977.tb01280.x

By:

Gustavson, K.-H.;
Wahlström, J.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1977, v. 11, n. 1, p. 78, doi. 10.1111/j.1399-0004.1977.tb01283.x
Publication type:: Article