Works matching IS 00099163 AND DT 1980 AND VI 17 AND IP 2

Results: 15

Baller-Gerold syndrome Craniosynostosis-radial aplasia syndrome.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 161, doi. 10.1111/j.1399-0004.1980.tb00126.x

By:

Anyane-Yeboa, K.;
Gunning, L.;
Bloom, A. D.

Publication type:

Article

Bloom's syndrome in a Japanese girl.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 143, doi. 10.1111/j.1399-0004.1980.tb00123.x

By:

Kawashima, Hiroko;
Sato, Tamotu;
Taniguchi, Noboru;
Yagl, Takashi;
Ishizaki, Kanzi;
Takere, Hiraku

Publication type:

Article

Familial X-linked mental retardation with a marker X chromosome and its relationship to macro-orchidism.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 125, doi. 10.1111/j.1399-0004.1980.tb00120.x

By:

Howard-Peebles, Patricia N.;
Stoddard, Gayle R.

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1980, v. 17, n. 2, p. 176, doi. 10.1111/j.1399-0004.1980.tb00129.x
Publication type:: Article

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 129, doi. 10.1111/j.1399-0004.1980.tb00121.x

By:

Mattei, J. F.;
Mattei, M. G.;
Ardissone, J. P.;
Taramasco, H.;
Giraud, F.

Publication type:

Article

Dermatoglyphic patterns in the Sjögren-Larsson syndrome.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 120, doi. 10.1111/j.1399-0004.1980.tb00119.x

By:

Gustavson, K. H.;
Jagell, S.

Publication type:

Article

The calculation of genetic risks in X-linked recessive conditions using programmable calculators.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 171, doi. 10.1111/j.1399-0004.1980.tb00128.x

By:

Winter, R. M.

Publication type:

Article

Association of severe rheumatoid arthritis with heterozygosity for α-antitrypsin deficiency.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 153, doi. 10.1111/j.1399-0004.1980.tb00125.x

By:

Cox, Diane Wilson;
Huber, Olga

Publication type:

Article

Upper limb anomalies and renal disease.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 117, doi. 10.1111/j.1399-0004.1980.tb00118.x

By:

Siegler, Richard L.;
Larsen, Paul;
Buehler, Bruce A.

Publication type:

Article

Absent ulna in the Klippel-Feil syndrome: an unusual associated malformation.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 167, doi. 10.1111/j.1399-0004.1980.tb00127.x

By:

Chemke, J.;
Nisani, R.;
Fischel, R. E.

Publication type:

Article

Gc Serum groups and schizophrenia.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 149, doi. 10.1111/j.1399-0004.1980.tb00124.x

By:

Beckman, L.;
Beckman, G.;
Perris, C.

Publication type:

Article

Penetrance estimates and recurrence risks for fibromuscular dysplasia.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 115, doi. 10.1111/j.1399-0004.1980.tb00117.x

By:

Gladstien, K.;
Rushton, A. R.;
Kidd, K. K.

Publication type:

Article

The spectrum of frontonasal dysplasia in an inbred pedigree.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 137, doi. 10.1111/j.1399-0004.1980.tb00122.x

By:

Fuenmayor, H. Moreno

Publication type:

Article

Spontaneous and X-ray induced chromosomal aberrations in selected connective tissue diseases.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 108, doi. 10.1111/j.1399-0004.1980.tb00116.x

By:

Burkhardt, Wesley C.;
Jackson, John F.;
Songcharoen, Suthin;
Meydrech, Edward F.

Publication type:

Article

Dominant sex-linked inherited chondrodysplasia punctata: a distinct type of chondrodysplasia punctata.

Published in:

Clinical Genetics, 1980, v. 17, n. 2, p. 97, doi. 10.1111/j.1399-0004.1980.tb00115.x

By:

Manzke, H.;
Christophers, E.;
Wiedemann, H.-R.

Publication type:

Article