Works matching IS 00099163 AND DT 1975 AND VI 7 AND IP 4

Results: 15

Lp(a) lipoprotein/pre-ß.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 334, doi. 10.1111/j.1399-0004.1975.tb00338.x

By:

Dahlén, G.;
Berg, K.;
Gillnäs, T.;
Ericson, C.

Publication type:

Article

Investigations on Huntington's disease in the Canadian Prairies.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 345, doi. 10.1111/j.1399-0004.1975.tb00340.x

By:

Shokeir, M. H. K.

Publication type:

Article

Investigation on Huntington's disease in the Canadian Prairies.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 349, doi. 10.1111/j.1399-0004.1975.tb00341.x

By:

Shokeir, M. H. K.

Publication type:

Article

Familial balanced (7;11;21)translocation and Down's syndrome in two siblings.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 304, doi. 10.1111/j.1399-0004.1975.tb00333.x

By:

Schwinger, E.;
Mikkelen, Margareta;
Niesen, Mathilda

Publication type:

Article

Materno-fetal ABO incompatibility as a cause of spontaneous abortion.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 308, doi. 10.1111/j.1399-0004.1975.tb00334.x

By:

Lauritsen, J. Glenn;
Grunnet, N.;
Jensen, O. Myhre

Publication type:

Article

The Unique Green phenomenon and colour vision.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 274, doi. 10.1111/j.1399-0004.1975.tb00329.x

By:

Cobb, Stephen R.

Publication type:

Article

Investigation on Huntington's disease.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 354, doi. 10.1111/j.1399-0004.1975.tb00342.x

By:

Shokeir, M. H. K.

Publication type:

Article

Dominant mesomelic dwarfism of the hypoplastic tibia, radius type.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 280, doi. 10.1111/j.1399-0004.1975.tb00330.x

By:

Leroy, J. G.;
Vos, J. De;
Timmermans, J.

Publication type:

Article

Focal dermal hypoplasia syndrome in a male.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 325, doi. 10.1111/j.1399-0004.1975.tb00336.x

By:

Toro-Sola, Maria A.;
Kistenmacher, Mildred L.;
Punnett, Hope H.;
DiGeorge, Angelo M.

Publication type:

Article

Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 299, doi. 10.1111/j.1399-0004.1975.tb00332.x

By:

Yanagisawa, Satoshi;
Yokoyama, Hiroshi

Publication type:

Article

Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 261, doi. 10.1111/j.1399-0004.1975.tb00328.x

By:

Blank, C. E.;
Colver, Doreen C. B.;
Potter, A. M.;
McHugh, J.;
Lorber, J.

Publication type:

Article

Linkage investigation of a large family with Reifenstein's syndrome.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 342, doi. 10.1111/j.1399-0004.1975.tb00339.x

By:

Ott, Jurg;
Goldstein, Joseph L.;
Harrod, Mary I.

Publication type:

Article

Trisomy 9p in a patient with a de novo 9/15 translocation.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 317, doi. 10.1111/j.1399-0004.1975.tb00335.x

By:

Jacobsen, Petrea;
Hobolth, Niels;
Mikkelsen, Margareta

Publication type:

Article

Two cases of 8p trisomy in one sibship.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 328, doi. 10.1111/j.1399-0004.1975.tb00337.x

By:

Chiyo, Hide-Aki;
Nakagome, Yasuo;
Matsui, Ichiro;
Kuroki, Yoshikazu;
Kobayash, Hideo;
Ono, Kazuo

Publication type:

Article

Friedreich's ataxia in Western Norway.

Published in:

Clinical Genetics, 1975, v. 7, n. 4, p. 287, doi. 10.1111/j.1399-0004.1975.tb00331.x

By:

Skre, Håvard

Publication type:

Article