Works matching IS 00099163 AND DT 1974 AND VI 6 AND IP 2

Results: 11

Concordance rates for myopia in twins.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 142, doi. 10.1111/j.1399-0004.1974.tb00643.x

By:

Karlsson, Jon L.

Publication type:

Article

Detection of inborn errors of metabolism.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 73, doi. 10.1111/j.1399-0004.1974.tb00634.x

By:

Hill, Helene Z.;
Goodman, Stephen I.

Publication type:

Article

A case with 46, XX, del (11) (q21).

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 90, doi. 10.1111/j.1399-0004.1974.tb00637.x

By:

Faust, J.;
Vogel, W.;
Löning, B.

Publication type:

Article

Hyperglycinuria in a family with autosomal dominantly inherited cataract.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 138, doi. 10.1111/j.1399-0004.1974.tb00642.x

By:

Similä, Seppo;
Käär, Maria-Lhsa

Publication type:

Article

Genetic and clinical aspects of Charcot-Marie-Tooth's disease.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 98, doi. 10.1111/j.1399-0004.1974.tb00638.x

By:

Skre, H.

Publication type:

Article

Hepatic fibrosis, polycystic kidney, colobomata and encephalopathy in siblings.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 82, doi. 10.1111/j.1399-0004.1974.tb00636.x

By:

Hunter, Alasdair G. W.;
Rothman, Stanley J.;
Hwang, Wei Sek;
Deckelbaum, Richard J.

Publication type:

Article

The Aarskog syndrome in three brothers.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 119, doi. 10.1111/j.1399-0004.1974.tb00639.x

By:

Funderburk, Steve J.;
Crandall, Barbara F.

Publication type:

Article

Detection of inborn errors of metabolism.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 79, doi. 10.1111/j.1399-0004.1974.tb00635.x

By:

Hill, Helene Z.;
Goodman, Stephen I.

Publication type:

Article

Electromyography of oral-facial musculature in craniocarpaltarsal dysplasia (Freeman-Sheldon syndrome).

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 132, doi. 10.1111/j.1399-0004.1974.tb00641.x

By:

Jr, John J. Sauk;
Delaney, James R.;
Reaume, Charles;
Brandjord, Robert;
Jr, Carl J. Witkop

Publication type:

Article

47, XY, t(9p+;11q+) in a male infant with multiple malformations.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 125, doi. 10.1111/j.1399-0004.1974.tb00640.x

By:

Dinno, Nuhad D.;
Silvey, Gary L.;
Weisskopf, Bernard

Publication type:

Article

A linkage study of phenylketonuria.

Published in:

Clinical Genetics, 1974, v. 6, n. 2, p. 147, doi. 10.1111/j.1399-0004.1974.tb00644.x

By:

Berg, Kare;
Saugstad, Letten Fegersten

Publication type:

Article