Works matching IS 00099163 AND DT 1982 AND VI 21 AND IP 4

Results: 13

Note added in proof.

Published in:: Clinical Genetics, 1982, v. 21, n. 4, p. 271, doi. 10.1111/j.1399-0004.1982.tb00762.x
Publication type:: Article

Metachromatic leukodystrophy caused by a partial cerebroside sulfatase defect.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 253, doi. 10.1111/j.1399-0004.1982.tb00759.x

By:

Kihara, Hayato;
Fluharty, Arvan L.;
O'Brien, John S.;
Fish, Charles H.

Publication type:

Article

Ring chromosome 15: Report of a case in an infertile man.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 272, doi. 10.1111/j.1399-0004.1982.tb00763.x

By:

Moreau, Nicole;
Teyssier, Michelle

Publication type:

Article

Ichthyosis in the Sjögren-Larsson syndrome.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 243, doi. 10.1111/j.1399-0004.1982.tb00758.x

By:

Jagell, S.;
Lidén, S.

Publication type:

Article

Mucolipidosis II: unusual presentation with a congenital angulated fracture.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 225, doi. 10.1111/j.1399-0004.1982.tb00754.x

By:

Michels, Virginia V.;
Dutton, Robert V.;
Caskey, C. Thomas

Publication type:

Article

Heterogeneity and pleiotropism in the Moebius syndrome Sirs.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 290, doi. 10.1111/j.1399-0004.1982.tb00765.x

By:

Baraitser, Michael

Publication type:

Article

Mosaic tetrasomy 21 in a liveborn male infant.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 228, doi. 10.1111/j.1399-0004.1982.tb00755.x

By:

Hunter, Alasdair G. W.;
Clifford, Brian;
Speevak, Marsha;
MacMurray, S. Brock

Publication type:

Article

C-heteromorphism in the human X-chromosome Sirs.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 290, doi. 10.1111/j.1399-0004.1982.tb00766.x

By:

Friedrich, Ursula

Publication type:

Article

The effect of variant chromosomes on reproductive fitness in man.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 280, doi. 10.1111/j.1399-0004.1982.tb00764.x

By:

Carothers, Andrew D.;
Buckton, Karin E.;
Collyer, Susan;
Mey, Rhona de;
Frackiewicz, Anna;
Piper, James;
Smith, Lynne

Publication type:

Article

Pure XX gonadal dysgenesis in identical twins.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 262, doi. 10.1111/j.1399-0004.1982.tb00760.x

By:

Youlton, Ronald;
Michelsen, Harold;
Be, Cecilia;
Cruz-Coke, Ricardo

Publication type:

Article

Heterogeneity of insulin-dependent diabetes-new evidence.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 233, doi. 10.1111/j.1399-0004.1982.tb00756.x

By:

Dunsworth, T. S.;
Rich, S. S.;
Morton, N. E.;
Barbosa, J.

Publication type:

Article

A familial pericentric inversion of chromosome 8 analysed with a high resolution chromosome banding technique.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 266, doi. 10.1111/j.1399-0004.1982.tb00761.x

By:

Bui, The-Hung;
Sichong, Zhang;
Castro, Isabel

Publication type:

Article

Fetal dermatoglyphics.

Published in:

Clinical Genetics, 1982, v. 21, n. 4, p. 237, doi. 10.1111/j.1399-0004.1982.tb00757.x

By:

Katznelson, M. Bat-Miriam;
Goldman, B.

Publication type:

Article