Works matching IS 00099163 AND DT 1975 AND VI 7 AND IP 3

Results: 12

A case of trisomy 8 mosaicism 47, XX, + 8/46, XX.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 232, doi. 10.1111/j.1399-0004.1975.tb00324.x

By:

Aller, V.;
Abrisqueta, J. A.;
Perez, A.;
Martin, M. A.;
Goday, C.;
Mazo, J. Del

Publication type:

Article

Ring chromosome 13 syndrome.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 203, doi. 10.1111/j.1399-0004.1975.tb00320.x

By:

Fried, K.;
Rosenblatt, M.;
Mundel, G.;
Krikler, R.

Publication type:

Article

Genetics of the GPT system. Family, mother/child and association studies.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 245, doi. 10.1111/j.1399-0004.1975.tb00326.x

By:

Olaisen, Blørner

Publication type:

Article

Polycythemia Vera treated with.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 227, doi. 10.1111/j.1399-0004.1975.tb00323.x

By:

Stavem, Per;
Hagen, Carl B. van der;
Vogt, Else;
Sandnes, Kjell

Publication type:

Article

Familial occurrence of the G syndrome.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 238, doi. 10.1111/j.1399-0004.1975.tb00325.x

By:

Biervliet, J. P. G. M. Van;
Hemel, J. O. van

Publication type:

Article

The significance of 'unspecific neuropathy' in hereditary ataxias and related disorders.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 209, doi. 10.1111/j.1399-0004.1975.tb00321.x

By:

Skre, Håvard

Publication type:

Article

Familial amyotrophic lateral sclerosis with dementia: A second Canadian family.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 186, doi. 10.1111/j.1399-0004.1975.tb00317.x

By:

Pinsky, Leonard;
Finlayson, M. H.;
Libman, I.;
Scott, B. H.

Publication type:

Article

Evidence for recessive inheritance of myopia.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 197, doi. 10.1111/j.1399-0004.1975.tb00319.x

By:

Karlsson, Jon L.

Publication type:

Article

Asymmetric septal hypertrophy in a large Amish kindred.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 255, doi. 10.1111/j.1399-0004.1975.tb00327.x

By:

Bingle, J.;
Dillon, James;
Hurwitz, Roger

Publication type:

Article

X-linked hypoxanthine-guanine phosphoribosyltransferase deficiency without neurological disorders. A report of a family.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 181, doi. 10.1111/j.1399-0004.1975.tb00316.x

By:

Toyo-Oka, Teruhiko;
Hanaoka, Fumo;
Akaoka, Ieo;
Yamada, Masa-Atsu

Publication type:

Article

Mental retardation and congenital malformations associated with a ring chromosome 6.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 192, doi. 10.1111/j.1399-0004.1975.tb00318.x

By:

Fried, K.;
Rosenblatt, M.;
Mundel, G.;
Krikler, R.

Publication type:

Article

A computer-oriented linkage analysis scheme.

Published in:

Clinical Genetics, 1975, v. 7, n. 3, p. 219, doi. 10.1111/j.1399-0004.1975.tb00322.x

By:

Freidhoff, Linda B.;
Chase, Gary

Publication type:

Article