Works matching IS 00099163 AND DT 1977 AND VI 12 AND IP 3

Results: 11

Interchromosomal effects in man.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 189, doi. 10.1111/j.1399-0004.1977.tb00924.x

By:

Hecht, Frederick;
Patil, Shivanand R.

Publication type:

Article

Medical Geneticist.

Published in:: Clinical Genetics, 1977, v. 12, n. 3, p. 191, doi. 10.1111/j.1399-0004.1977.tb00925.x
Publication type:: Article

Bloom's syndrome. V. Surveillance for cancer in affected families.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 162, doi. 10.1111/j.1399-0004.1977.tb00919.x

By:

German, James;
Bloom, David;
Passarge, Eberhard

Publication type:

Article

Major karyotypic abnormality in a child born to a woman with untreated malignant melanoma.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 155, doi. 10.1111/j.1399-0004.1977.tb00918.x

By:

Fitzgerald, P. H.;
Miethke, Patricia;
Caseley, R. T.

Publication type:

Article

Apparently balanced de novo translocations in patients with abnormal phenotypes.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 188, doi. 10.1111/j.1399-0004.1977.tb00923.x

By:

Jongbloet, P. H.;
Erkelens-Zwets, J. H. J.

Publication type:

Article

The foetus in Duchenne muscular dystrophy: Muscle growth in tissue culture.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 183, doi. 10.1111/j.1399-0004.1977.tb00922.x

By:

Emery, Alan E. H.;
McGregor, Louise

Publication type:

Article

Mydriasis and heredity.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 129, doi. 10.1111/j.1399-0004.1977.tb00915.x

By:

Goldsmith, Robert I.;
Rothhammer, Francisco;
Schull, William J.

Publication type:

Article

On the classification of the acrocephalosyndactyly syndromes.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 169, doi. 10.1111/j.1399-0004.1977.tb00920.x

By:

Escobar, Victor;
Bixler, David

Publication type:

Article

Studies on the metabolic defect in Broad-ß disease (hyperlipoproteinaemia type III).

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 139, doi. 10.1111/j.1399-0004.1977.tb00917.x

By:

Utermann, G.;
Canzler, H.;
Hees, M.;
Jaeschke, M.;
Mühlfellner, G.;
Schoenborn, W.;
Vogelberg, K. H.

Publication type:

Article

The Stickler syndrome (Hereditary arthro-ophthalmopathy).

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 179, doi. 10.1111/j.1399-0004.1977.tb00921.x

By:

Say, Burhan;
Berry, Judy;
Barber, Nancy

Publication type:

Article

Hereditary cholinesterase deficiency: A report of a family with two rare genotypes.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 134, doi. 10.1111/j.1399-0004.1977.tb00916.x

By:

Baker, Edward L.;
Smrek, Ann;
Kimbrough, Renate D.;
Hudgins, Michael;
Landrigan, Philip J.;
Liddle, John A.

Publication type:

Article