Works matching IS 00099163 AND DT 1974 AND VI 5 AND IP 3

Results: 14

X/XY mosaicism with short Y.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 211, doi. 10.1111/j.1399-0004.1974.tb01684.x

By:

Berger, R.;
Relier, J. P.;
Salmon, Ch.;
Minkowski, A.

Publication type:

Article

The relation of the sex of choreic and rigid subjects to the age at onset of Huntington's disease.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 248, doi. 10.1111/j.1399-0004.1974.tb01690.x

By:

Brackenridge, C. J.;
Chamberlin, M.

Publication type:

Article

Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, +21/46, X, +21 karyotype.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 259, doi. 10.1111/j.1399-0004.1974.tb01692.x

By:

Mello, R. Santos;
Souza, O. A.;
Santos Mello, E. M. K. Sz;
Pimentel, E. C.

Publication type:

Article

Cerebellar ataxia and total albinism: A kindred suggesting pleiotropism or linkage.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 196, doi. 10.1111/j.1399-0004.1974.tb01682.x

By:

Skre, H.;
Berg, K.

Publication type:

Article

Case report of an extra, small, acrocentric chromosome in a non-mongoloid girl.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 254, doi. 10.1111/j.1399-0004.1974.tb01691.x

By:

Kaijser, Kurt

Publication type:

Article

Partial trisomy 13 in a case of Cyclopia with 13/14 translocation.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 218, doi. 10.1111/j.1399-0004.1974.tb01685.x

By:

Singh, D. N.;
Wiscovitch, R. A.;
Osborne, R. A.;
Hennigar, G. R.

Publication type:

Article

Genetic counseling: an appraisal.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 177, doi. 10.1111/j.1399-0004.1974.tb01680.x

By:

Reynolds, Beverly Dev.;
Puck, Mary H.;
Robinson, Arthur

Publication type:

Article

A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t (6;19).

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 188, doi. 10.1111/j.1399-0004.1974.tb01681.x

By:

Pallister, P. D.;
Patau, K.;
Inhorn, S. L.;
Opitz, J. M.

Publication type:

Article

Idiopathic haemochromatosis and diabetes mellitus.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 242, doi. 10.1111/j.1399-0004.1974.tb01689.x

By:

Saddi, R.;
Feinoold, J.

Publication type:

Article

Muscle histology in fetuses at risk for Duchenne muscular dystrophy.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 230, doi. 10.1111/j.1399-0004.1974.tb01687.x

By:

Toop, James;
Emery, Alan E. H.

Publication type:

Article

The genetic entity of hypochondroplasia.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 223, doi. 10.1111/j.1399-0004.1974.tb01686.x

By:

Frydman, M.;
Hertz, M.;
Goodman, R. M.

Publication type:

Article

An infant with an XXXYY karyotype.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 263, doi. 10.1111/j.1399-0004.1974.tb01693.x

By:

Bilt, F. A. Lecluse-;
Hagemeijer, A.;
Smit, E. M. E.;
Visser, H. K. A.;
Vaandrager, G. J.

Publication type:

Article

Idiopathic haemochromatosis: An autosomal recessive disease.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 234, doi. 10.1111/j.1399-0004.1974.tb01688.x

By:

Saddi, R.;
Feingold, J.

Publication type:

Article

Incidence of chromosome aberrations in a child psychiatric hospital.

Published in:

Clinical Genetics, 1974, v. 5, n. 3, p. 205, doi. 10.1111/j.1399-0004.1974.tb01683.x

By:

Christensen, K. R.;
Nielsen, J.

Publication type:

Article