Works matching IS 00099163 AND DT 1979 AND VI 16 AND IP 1

Results: 11

Counseling problems when twins are discovered at genetic amniocentesis.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 34, doi. 10.1111/j.1399-0004.1979.tb00846.x

By:

Hunter, AlasdairG. W.;
Cox, DavidM.

Publication type:

Article

XY sex-reversed campomelia - possibly an X-linked disorder?

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 62, doi. 10.1111/j.1399-0004.1979.tb00852.x

By:

Schimke, R. Neil

Publication type:

Article

Hallervorden-Spatz disease.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 1, doi. 10.1111/j.1399-0004.1979.tb00842.x

By:

Elejalde, B. Rafael;
Elejalde, MariaMercedesJ. de;
Lopez, Federico

Publication type:

Article

A new presumably autosomal recessive form of the Ehlers-Danlos syndrome.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 19, doi. 10.1111/j.1399-0004.1979.tb00843.x

By:

Beasley, R. Palmer;
Cohen, M. Michael

Publication type:

Article

A patient with a 47, XXY,5p- karyotype.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 43, doi. 10.1111/j.1399-0004.1979.tb00847.x

By:

Palevsky, S.;
Radfar, N.;
Pan, S.;
Steele, M. W.

Publication type:

Article

Distal trisomy 17q.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 54, doi. 10.1111/j.1399-0004.1979.tb00849.x

By:

Turleau, C.;
Grouchy, J.;
Bouveret, J. P.

Publication type:

Article

Partial trisomy 12q associated with a familial translocation.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 25, doi. 10.1111/j.1399-0004.1979.tb00844.x

By:

Hemming, Lorraine;
Brown, Richard

Publication type:

Article

Recurrence risks for congenital hydrocephalus.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 47, doi. 10.1111/j.1399-0004.1979.tb00848.x

By:

Burton, BarbaraK.

Publication type:

Article

Genetic markers in individuals with a 5p- karyotype.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 58, doi. 10.1111/j.1399-0004.1979.tb00850.x

By:

Fenger, K.;
MØHL, I. A.

Publication type:

Article

Alcohol metabolizing enzymes: Studies of isozymes in human biopsies and cultured fibroblasts.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 29, doi. 10.1111/j.1399-0004.1979.tb00845.x

By:

Goedde, H. W.;
Agarwal, D. P.;
Harada, S.

Publication type:

Article

Prenatal diagnosis of sialidosis with combined neuraminidase and ø-galactosidase deficiency.

Published in:

Clinical Genetics, 1979, v. 16, n. 1, p. 60, doi. 10.1111/j.1399-0004.1979.tb00851.x

By:

Kleijer, W. J.;
Hoogeveen, A.;
Verheijen, F. W.;
Niermeijer, M. F.;
Galjaard, H.;
O'Brien, J. S.;
Warner, T. G.

Publication type:

Article