Works matching IS 00099163 AND DT 1980 AND VI 17 AND IP 6

Results: 13

Elimination of an abnormal cell line from blood lymphocytes during post-natal growth.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 433, doi. 10.1111/j.1399-0004.1980.tb00176.x

By:

Fitzgerald, Peter H.;
Mercer, Jan M.

Publication type:

Article

Genetic association in vitiligo: ABO, MNSs, Rhesus, KeII and Duffy blood groups.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 415, doi. 10.1111/j.1399-0004.1980.tb00172.x

By:

Wasfi, A. I.;
Saha, N.;
Munshid, H. A. El;
Sheikh, F. S. El;
Ahmed, M. A.

Publication type:

Article

A new white forelock (poliosis) syndrome with multiple congenital malformations in two sibs.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 437, doi. 10.1111/j.1399-0004.1980.tb00177.x

By:

Goodman, R. M.;
Yahav, Y.;
Frand, M.;
Barzilay, Z.;
Nissan, E.;
Hertz, M.

Publication type:

Article

Hereditary ataxia in a large Danish pedigree.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 385, doi. 10.1111/j.1399-0004.1980.tb00168.x

By:

Pedersen, Lene

Publication type:

Article

Forsius-Eriksson syndrome: Its relation to the Nettleship-Falls X-linked ocular albinism.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 403, doi. 10.1111/j.1399-0004.1980.tb00170.x

By:

O'Donnell, F. E.;
Green, W. R.;
McKusick, V. A.;
Forsius, H.;
Eriksson, A. W.

Publication type:

Article

The use of genetic linkage in counselling families with dystrophia myotonica.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 443, doi. 10.1111/j.1399-0004.1980.tb00178.x

By:

Gibson, Sheila L. M.;
Ferguson-Smith, M. A.

Publication type:

Article

Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 418, doi. 10.1111/j.1399-0004.1980.tb00173.x

By:

Palmer, Catherine G.;
Schwartz, Stuart;
Hodes, M. E.

Publication type:

Article

Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32→13qter.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 428, doi. 10.1111/j.1399-0004.1980.tb00175.x

By:

Telfer, M. A.;
Clark, C. E.;
Casey, P. A.;
Cowell, H. R.;
Stroud, H. H.

Publication type:

Article

Risk factors associated with neural tube defects.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 394, doi. 10.1111/j.1399-0004.1980.tb00169.x

By:

McCormack, Michael K.;
Breslin, Nancy;
Coppola-McCormack, Patricia J.

Publication type:

Article

Detection of Lesch-Nyhan Syndrome Carriers: Analysis of hair roots for HPRT by agarose gel electrophoresis and autoradiography.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 369, doi. 10.1111/j.1399-0004.1980.tb00166.x

By:

Bakay, Bohdan;
Tucker-Pian, Charmaine;
Seegmiller, J. E.

Publication type:

Article

A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 423, doi. 10.1111/j.1399-0004.1980.tb00174.x

By:

Guanti, Ginevra

Publication type:

Article

Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 409, doi. 10.1111/j.1399-0004.1980.tb00171.x

By:

McCorquodale, M.;
Erickson, R. P.;
Robinson, M.;
Roszczipka, K.

Publication type:

Article

The Wolf-Hirschhorn syndrome.

Published in:

Clinical Genetics, 1980, v. 17, n. 6, p. 375, doi. 10.1111/j.1399-0004.1980.tb00167.x

By:

Lurie, I. W.;
Lazjuk, G. I.;
Usaova, Y. I.;
Presman, E. B.;
Gurevich, D. B.

Publication type:

Article