Works matching IS 00099163 AND DT 1973 AND VI 4 AND IP 5

Results: 15

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 434, doi. 10.1111/j.1399-0004.1973.tb01173.x

By:

Jacobsen, Petrea;
Mikkelsen, Margareta;
Rosleff, Flemming

Publication type:

Article

Prevalence of chromosome abnormalities among males examined for military service.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 422, doi. 10.1111/j.1399-0004.1973.tb01171.x

By:

Zeuthen, Eva;
Nielsen, Johannes

Publication type:

Article

Presumptive fluorescent evidence for spermatocyte with X+Y+Y diakinetic univalents in an XYY male.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 415, doi. 10.1111/j.1399-0004.1973.tb01169.x

By:

Luciani, J. M.;
Vagner-Capodano, Anne-Marie;
Devictor-Vuillet, Monique;
AUBERT, L.;
STAHL, A.

Publication type:

Article

Dermatoglyphics in Down's syndrome. III.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 381, doi. 10.1111/j.1399-0004.1973.tb01164.x

By:

Deckers, J. F. M.;
Oorthuys, A. M. A.;
Doesburg, W. H.

Publication type:

Article

Isochromosome Y [46, X, i(Yq)] and female phenotype.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 410, doi. 10.1111/j.1399-0004.1973.tb01168.x

By:

Böök, J. A.;
Eilon, Batia;
Halbrecht, I.;
Komlos, Luise;
Shabtay, Fiorella

Publication type:

Article

A comparative study of different electrophoretic techniques for classification of hereditary hyperlipoproteinaemias.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 450, doi. 10.1111/j.1399-0004.1973.tb01176.x

By:

Heiberg, Arvid

Publication type:

Article

Studies in Down's syndrome.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 407, doi. 10.1111/j.1399-0004.1973.tb01167.x

By:

Rittner, Ch.;
Rittner, Beate

Publication type:

Article

Frequency and morphology of the Y-body in patients with female or ambisexual phenotype.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 447, doi. 10.1111/j.1399-0004.1973.tb01175.x

By:

Schwinger, E.;
Bcczkowski, K.

Publication type:

Article

Familial laryngeal abductor paralysis and psychomotor retardation.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 429, doi. 10.1111/j.1399-0004.1973.tb01172.x

By:

Watters, Gordon V.;
Fitch, Naomi

Publication type:

Article

Mucolipidosis III (pseudo-Hurler polydystrophy): Cytological and ultrastructural observations of cultured fibroblast cells.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 388, doi. 10.1111/j.1399-0004.1973.tb01165.x

By:

Taylor, H. A.;
Thomas, G. H.;
Miller, C. S.;
Kelly, T. E.;
Siggers, D.

Publication type:

Article

Metachromatic leukodystrophy.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 442, doi. 10.1111/j.1399-0004.1973.tb01174.x

By:

Børresen, Anne-Lise;
Hagen, C. B. Van Der

Publication type:

Article

A girl with severe expression of the Holt-Oram gene.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 417, doi. 10.1111/j.1399-0004.1973.tb01170.x

By:

Gardner, R. J. M.;
Buckfield, Patricia M.;
Veale, A. M. O.

Publication type:

Article

Rapid tissue culture and microbiochemical methods for analyzing colonially grown fibroblasts from normal, Lesch-Nyhan and Tay-Sachs patients and amniotic fluid cells.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 376, doi. 10.1111/j.1399-0004.1973.tb01163.x

By:

Richardson, B. J.;
Cox, D. M.

Publication type:

Article

Studies in Down's syndrome.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 398, doi. 10.1111/j.1399-0004.1973.tb01166.x

By:

Rittner, Ch.;
Schwinger, E.

Publication type:

Article

The lobster claw defect with ectodermal defects, cleft lip-palate, tear duct anomaly and renal anomalies.

Published in:

Clinical Genetics, 1973, v. 4, n. 5, p. 369, doi. 10.1111/j.1399-0004.1973.tb01162.x

By:

Preus, M.;
Fraser, F. C.

Publication type:

Article