Works matching IS 00099163 AND DT 1989 AND VI 35 AND IP 6

Results: 15

Linkage in a family with X-linked Charcot-Marie-Tooth disease.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 399, doi. 10.1111/j.1399-0004.1989.tb02964.x

By:

Haites, N.;
Fairweather, N.;
Clark, C.;
Kelly, K. F.;
Simpson, S.;
Johnston, A. W.

Publication type:

Article

Mosaic 47,XY, + 8/48,XXYY in a mentally non-retarded man with phenotypical and neurological abnormalities.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 446, doi. 10.1111/j.1399-0004.1989.tb02970.x

By:

Hoovers, J. M. N.;
Oorthuys, J. W. E.;
Visser, M.

Publication type:

Article

X-linked olivopontocerebellar atrophy.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 417, doi. 10.1111/j.1399-0004.1989.tb02966.x

By:

Lutz, R.;
Bodensteiner, J.;
Schaffer, B.;
Gay, C.

Publication type:

Article

A non-enzymatic method for identification of citrullinemia heterozygotes.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 468, doi. 10.1111/j.1399-0004.1989.tb02975.x

By:

Clemens, Peter C.;
Plettner, Ch.

Publication type:

Article

Determining zygosity in the Vietnam Era Twin Registry: an approach using questionnaires.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 423, doi. 10.1111/j.1399-0004.1989.tb02967.x

By:

Eisen, S.;
Neuman, R.;
Goldberg, J.;
Rice, J.;
True, W.

Publication type:

Article

Partial duplication of the eyebrows with other congenital malformations: a new syndrome.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 467, doi. 10.1111/j.1399-0004.1989.tb02974.x

By:

Gross-Kieselstein, Eva;
Har-Even, Yehuda

Publication type:

Article

Duchenne muscular dystrophy:detection of deletion carriers by spectrophotometric densitometry.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 393, doi. 10.1111/j.1399-0004.1989.tb02963.x

By:

Laing, Nigel G.;
Siddique, Teepu;
Bartlett, Richard;
Yamaoka, Larry H.;
Hung, Wu-Yen;
Pericak-Vance, Margaret A.;
Roses, Allen D.

Publication type:

Article

X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a female.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 462, doi. 10.1111/j.1399-0004.1989.tb02973.x

By:

Turleau, Catherine;
Niaudet, P.;
Cabanis, Marie-Odile;
Plessis, Ghislaine;
Cau, D.;
Grouchy, J.

Publication type:

Article

Unique inheritance of streptomycininduced deafness.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 433, doi. 10.1111/j.1399-0004.1989.tb02968.x

By:

Higashi, Koichiro

Publication type:

Article

Genetic counseling in families with inherited balanced translocations: experience with 36 families.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 404, doi. 10.1111/j.1399-0004.1989.tb02965.x

By:

Wolff, Gerhard;
Back, Elke;
Arleth, Sybille;
Rapp-Körner, Uschi

Publication type:

Article

Ichthyosis with an unusual constellation of ectodermal dysplasias.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 455, doi. 10.1111/j.1399-0004.1989.tb02972.x

By:

Baden, Howard P.;
Imber, Michael

Publication type:

Article

'Variability gene' effect of cholesteryl ester transfer protein (CETP) genes.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 437, doi. 10.1111/j.1399-0004.1989.tb02969.x

By:

Berg, Kåre;
Kondo, Ikuko;
Drayna, Dennis;
Lawn, Richard

Publication type:

Article

A pseudoisochromosome 18q and an isodicentric chromosome 18.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 450, doi. 10.1111/j.1399-0004.1989.tb02971.x

By:

Floore, Cynthia;
Robertson, Anne;
Samuel, Iris;
Williamson, Nancy;
McLeod, D. R.;
Hoganson, G.;
Hoo, J. J.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1989, v. 35, n. 6, p. 472, doi. 10.1111/j.1399-0004.1989.tb02977.x
Publication type:: Article

Genetic heterogeneity of ataxia-telanglectasia.

Published in:

Clinical Genetics, 1989, v. 35, n. 6, p. 469, doi. 10.1111/j.1399-0004.1989.tb02976.x

By:

Hecht, Frederick;
Hecht, Barbara Kaiser McCaw

Publication type:

Article