Works matching IS 00099163 AND DT 1979 AND VI 15 AND IP 3

Results: 13

Acrocephalopolysyndactyly type IV: A new genetic syndrome in 3 sibs.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 209, doi. 10.1111/j.1399-0004.1979.tb00969.x

By:

Goodman, R. M.;
Sternberg, M.;
Shem-Tov, Y.;
Katznelson, M. Bat-Miriam;
Hertz, M.;
Rotem, Y.

Publication type:

Article

Craniometaphyseal dysplasia -variability of expression within a large family.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 252, doi. 10.1111/j.1399-0004.1979.tb00976.x

By:

Beighton, Peter;
Hamersma, Herman;
Horan, Frank

Publication type:

Article

Regional mapping of the HLA on the short arm of chromosome 6.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 245, doi. 10.1111/j.1399-0004.1979.tb00975.x

By:

Berger, R.;
Bernheim, A.;
Sasportes, M.;
Hauptmann, G.;
Hors, J.;
Legrand, L.;
Fellous, M.

Publication type:

Article

Prenatal diagnosis of trisomy 20 mosaicism.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 267, doi. 10.1111/j.1399-0004.1979.tb00978.x

By:

Kardon, Nataline B.;
Lieber, Ernest;
Davis, Jessica G.;
Hsu, Lillian Y. F.

Publication type:

Article

Prenatal diagnosis of polycystic kidneys and encephalocele (Meckel syndrome).

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 278, doi. 10.1111/j.1399-0004.1979.tb00980.x

By:

Friedrich, U.;
Hansen, K. Brogård;
Hauge, M.;
Hägerstrand, I.;
Kristoffersen, K.;
Ludvigsen, E.;
Merrild, U.;
Nørgaard-Pedersen, B.;
Petersen, G. Bruun;
Therkelsen, A. J.

Publication type:

Article

Epidermolysis bullosa simplex and mottled pigmentation: A new dominant syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 228, doi. 10.1111/j.1399-0004.1979.tb00972.x

By:

Fischer, T.;
Gedde-Dahl, T.

Publication type:

Article

X-linked dominant ichthyosis.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 239, doi. 10.1111/j.1399-0004.1979.tb00973.x

By:

Happle, Rudolf

Publication type:

Article

Familial occurrence of syngnathia congenita syndrome.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 241, doi. 10.1111/j.1399-0004.1979.tb00974.x

By:

Gassner, I.;
Müller, W.;
Rössler, H.;
Kofler, J.;
Mitterstieler, G.

Publication type:

Article

A supernumerary 'G' like chromosome originating from a maternal 13;15 translocation in a nondysmorphic, retarded girl.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 273, doi. 10.1111/j.1399-0004.1979.tb00979.x

By:

Wang, Hungshu;
Hunter, Alasdair G. W.

Publication type:

Article

Amniotic fluid cell culture.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 215, doi. 10.1111/j.1399-0004.1979.tb00970.x

By:

Felix, J. S.;
Doherty, R. A.

Publication type:

Article

Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 259, doi. 10.1111/j.1399-0004.1979.tb00977.x

By:

Maeda, Tohru;
Ohno, Michiko;
Takada, Masumi;
Nishida, Masato;
Tsukioka, Kazuko;
Tomjta, Hajime

Publication type:

Article

The human X-chromosome and the levels of serum immunoglobulin M.

Published in:

Clinical Genetics, 1979, v. 15, n. 3, p. 221, doi. 10.1111/j.1399-0004.1979.tb00971.x

By:

Escobar, Victor;
Corey, Linda A.;
Bixler, David;
Nance, Walter E.;
Biegei, Angenieta

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1979, v. 15, n. 3, p. 287, doi. 10.1111/j.1399-0004.1979.tb00981.x
Publication type:: Article