Works matching IS 00099163 AND DT 1979 AND VI 15 AND IP 1

Results: 15

Announcements.

Published in:: Clinical Genetics, 1979, v. 15, n. 1, p. 112, doi. 10.1111/j.1399-0004.1979.tb02035.x
Publication type:: Article

Chromosome breaks and sister chromatid exchanges in albinos in Nigeria.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 17, doi. 10.1111/j.1399-0004.1979.tb02024.x

By:

Cervenka, Jaroslav;
Witkop, Carl J.;
Okoro, Anezi N.;
King, Richard A.

Publication type:

Article

Isolated congenital ectopia lentis with autosomal dominant inheritance.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 97, doi. 10.1111/j.1399-0004.1979.tb02033.x

By:

Jaureouy, Beth M.;
Hall, Judith G.

Publication type:

Article

Polymorphism of apolipoprotein E.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 63, doi. 10.1111/j.1399-0004.1979.tb02028.x

By:

Utermann, G.;
Pruin, N.;
Steinmetz, A.

Publication type:

Article

Familial middle lobe bronchiectasis.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 85, doi. 10.1111/j.1399-0004.1979.tb02031.x

By:

Hoo, Joe Jie

Publication type:

Article

Dermatoglyphics in parents of children with trisomy 21.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 78, doi. 10.1111/j.1399-0004.1979.tb02030.x

By:

Ayme, Ségolène;
Mattei, Mark-Genevieve;
Mattei, J. F.;
Aurran, Yvette;
Giraud, F.

Publication type:

Article

A true hermaphrodite dispermic chimera with 46, XX and 46, XY karyotypes.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 89, doi. 10.1111/j.1399-0004.1979.tb02032.x

By:

Fitzgerald, P. H.;
Donald, R. A.;
Kirk, R. L.

Publication type:

Article

Prenatal diagnosis of the Meckel syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 1, doi. 10.1111/j.1399-0004.1979.tb02021.x

By:

Nevin, N. C.;
Thompson, W.;
Davison, G.;
Horner, W. T.

Publication type:

Article

Polymorphism of apolipoprotein E.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 37, doi. 10.1111/j.1399-0004.1979.tb02027.x

By:

Utermann, G.;
Vogelberg, K. H.;
Steinmetz, A.;
Schoenborn, W.;
Pruin, N.;
Jaeschke, M.;
Hees, M.;
Canzler, H.

Publication type:

Article

α.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 29, doi. 10.1111/j.1399-0004.1979.tb02026.x

By:

Lieberman, Jack;
Borhani, Nemat O.;
Feinleib, Manning

Publication type:

Article

No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45 XO Turner syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 22, doi. 10.1111/j.1399-0004.1979.tb02025.x

By:

Burns, Jane L.;
Hall, Judith G.;
Powers, Ellen;
Callis, James B.;
Hoehn, Holger

Publication type:

Article

Letter to the Editors.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 110, doi. 10.1111/j.1399-0004.1979.tb02034.x

By:

Kahler, Stephen G.;
Riley, Elizabeth

Publication type:

Article

Risk of malignancy and chromosomal polymorphism: a possible mechanism of association.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 73, doi. 10.1111/j.1399-0004.1979.tb02029.x

By:

Shabtai, Florella;
Halbrecht, Isaac

Publication type:

Article

Genetic structure of the Greek gypsies.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 5, doi. 10.1111/j.1399-0004.1979.tb02022.x

By:

Bartsocas, C. S.;
Karayanni, C.;
Tsipouras, P.;
Baibas, E.;
Bouloukos, A.;
Papadatos, C.

Publication type:

Article

Human gene mapping by postreduction and recombination frequencies under complete interference.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 11, doi. 10.1111/j.1399-0004.1979.tb02023.x

By:

Ott, Jurg

Publication type:

Article