Works matching IS 00099163 AND DT 1979 AND VI 15 AND IP 5

Results: 14

Announcement.

Published in:: Clinical Genetics, 1979, v. 15, n. 5, p. 464, doi. 10.1111/j.1399-0004.1979.tb01781.x
Publication type:: Article

Pi phenotypes of alpha.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 406, doi. 10.1111/j.1399-0004.1979.tb01772.x

By:

Arnaúd, Philippe;
Galbraith, Robert M.;
Faulk, W. Pagé;
Black, Carol

Publication type:

Article

XY gonadal dysgenesis associated with hGH and gonadotrophin deficiencies.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 369, doi. 10.1111/j.1399-0004.1979.tb01768.x

By:

Kauli, Rivka;
Pertzelan, Athaija;
Prager-Lewin, Ruth;
Maimon, Zipora;
Ovadia, Jardena;
Laron, Zvi

Publication type:

Article

Visual classification of banded human chromosomes.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 430, doi. 10.1111/j.1399-0004.1979.tb01775.x

By:

Lundsteen, Claes;
Granum, Erik

Publication type:

Article

Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patients.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 382, doi. 10.1111/j.1399-0004.1979.tb01770.x

By:

Norio, Reijo;
Koskiniemi, Marjaleena

Publication type:

Article

Trisomy 20 mosaicism in amniotic fluid cell culture.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 440, doi. 10.1111/j.1399-0004.1979.tb01776.x

By:

Nevin, N. C.;
Nevin, J.;
Thompson, W.

Publication type:

Article

Nonketotic hyperglycinemia A genetic study of 13 Finnish families.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 411, doi. 10.1111/j.1399-0004.1979.tb01773.x

By:

Wendt, L. V.;
Hirvasniemi, A.;
Similä, S.

Publication type:

Article

A New Osteosarcoma/Malformation Syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 462, doi. 10.1111/j.1399-0004.1979.tb01780.x

By:

Schuman, Stanley H.;
Burton, William E.

Publication type:

Article

A study of possible heterogeneity in Duchenne muscular dystrophy.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 444, doi. 10.1111/j.1399-0004.1979.tb01777.x

By:

Emery, Alan E. H.;
Skinner, Rosalind;
Holloway, Susan

Publication type:

Article

The technical variables associated with the frequencies of QFQ, RFA and CBG heteromorphisms of human chromosomes.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 450, doi. 10.1111/j.1399-0004.1979.tb01778.x

By:

Verma, Ram S.;
Dosik, Harvey

Publication type:

Article

Partial trisomy for the distal long arm of chromosome 5 (region q34→qter). A new clinically recognizable syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 454, doi. 10.1111/j.1399-0004.1979.tb01779.x

By:

Curry, Cynthia J. R.;
Loughman, William D.;
Francke, Uta;
Hall, Bryan D.;
Golbus, Mitchell S.;
Dersttne, Judy;
Epstein, Charles J.

Publication type:

Article

Description of chromosome banding patterns by band transition sequences.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 418, doi. 10.1111/j.1399-0004.1979.tb01774.x

By:

Lundsteen, Claes;
Granum, Erik

Publication type:

Article

Variability between and within laboratories in the analysis of structural chromosomal abnormalities.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 377, doi. 10.1111/j.1399-0004.1979.tb01769.x

By:

Zavala, C.;
Arroyo, P.;
Lisker, R.;
Carnevale, A.;
Salamanca, F.;
Navarrete, J. I.;
Jiménez, F. M.;
Blanco, B.;
Vázquez, V.;
Sánchez, J.;
Canún, S.

Publication type:

Article

Two XX male brothers.

Published in:

Clinical Genetics, 1979, v. 15, n. 5, p. 399, doi. 10.1111/j.1399-0004.1979.tb01771.x

By:

Minowada, Shioeru;
Kobayashi, Katsumi;
Isurugi, Koichiro;
Fukutani, Keiko;
Ikeuchi, Hiroko;
Hasegawa, Tomoko;
Yamada, Kiyomi

Publication type:

Article