Works matching IS 00099163 AND DT 1972 AND VI 3 AND IP 6

Results: 13

Dentinogenesis imperfecta: severe expression in a probable homozygote.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 442, doi. 10.1111/j.1399-0004.1972.tb01478.x

By:

Shokeir, M. H. K.

Publication type:

Article

Pseudo-achondrogenesis with fractures.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 435, doi. 10.1111/j.1399-0004.1972.tb01477.x

By:

Harris, R.;
Patton, J. T.;
Barson, A. J.

Publication type:

Article

Juvenile GM.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 411, doi. 10.1111/j.1399-0004.1972.tb01476.x

By:

O'Brien, J. S.;
Ho, M. W.;
Veath, M. L.;
Wilson, J. F.;
Myers, G.;
Opitz, J. M.;
Zurhein, G. M.;
Spranger, J. W.;
Hartmann, H. A.;
Haneberg, B.;
Grosses, F. R.

Publication type:

Article

8-trisomy in the bone marrow. Report of two cases.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 470, doi. 10.1111/j.1399-0004.1972.tb01483.x

By:

CHAPELLE, A. DE LA;
SCHRODER, J.;
VUOPIO, P.

Publication type:

Article

Some observations on the blood levels of phenylalanine in dilute mice and a comparison between human phenylketonuria and the disease of mice homozygous for the dilute lethal gene.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 495, doi. 10.1111/j.1399-0004.1972.tb01487.x

By:

Seller, Mary J.

Publication type:

Article

Variability in mongolism -a comparison of the hand skeleton in mongoloids and normals.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 452, doi. 10.1111/j.1399-0004.1972.tb01480.x

By:

Hall, Bertil;
Ringertz, Hans

Publication type:

Article

Attempted detection of heterozygotes for maple-syrup-urine disease.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 458, doi. 10.1111/j.1399-0004.1972.tb01481.x

By:

McKnight, Mary T.;
Spence, M. W.

Publication type:

Article

The relation of some features of Huntington's disease to the age at onset of symptoms in parents.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 477, doi. 10.1111/j.1399-0004.1972.tb01484.x

By:

Brackenridge, C. I.

Publication type:

Article

Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 490, doi. 10.1111/j.1399-0004.1972.tb01486.x

By:

Mallin, S. R.;
Walker, F. A.

Publication type:

Article

Australia antigen and Down's syndrome.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 448, doi. 10.1111/j.1399-0004.1972.tb01479.x

By:

Shiono, H.;
Kadowaki, J.;
Kasahara, S.;
Nakao, T.

Publication type:

Article

Zymograms of the human red cell acid phosphatase obtained with different substrates.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 483, doi. 10.1111/j.1399-0004.1972.tb01485.x

By:

SØRENSEN, S. A.

Publication type:

Article

Rheumatoid arthritis in the 46, XX, 18p- syndrome.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 465, doi. 10.1111/j.1399-0004.1972.tb01482.x

By:

Finley, Sara C.;
Finley, W. H.;
Johnson, J. C.;
Dodson, W. H.;
McPhee, H. T.

Publication type:

Article

PEDIG - A computer program for calculation of genotype probabilities using phenotype information.

Published in:

Clinical Genetics, 1972, v. 3, n. 6, p. 501, doi. 10.1111/j.1399-0004.1972.tb01488.x

By:

Heuch, Ivar;
Li, Francis H. F.

Publication type:

Article