Works matching IS 00099163 AND DT 1978 AND VI 14 AND IP 3

Results: 14

A 'new' autosomal dominant genodermatosis characterized by hyperpigmented spots and palmo- plantar hyperkeratosis.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 165, doi. 10.1111/j.1399-0004.1978.tb02123.x

By:

Cantú, J. M.;
Sánchez-Corona, J.;
Fragoso, R.;
Macotela-Ruiz, E.;
García-Cruz, D.

Publication type:

Article

Complete trisomy 22.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 139, doi. 10.1111/j.1399-0004.1978.tb02119.x

By:

Shokeir, M. H. K.

Publication type:

Article

Hazards of amniocentesis: An unidentifiable fragment.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 130, doi. 10.1111/j.1399-0004.1978.tb02117.x

By:

Lieber, Ernest;
Shah, Paloma;
Hack, Marilyn

Publication type:

Article

Dominant inheritance of multiple epiphyseal dysplasia, myopia and deafness.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 173, doi. 10.1111/j.1399-0004.1978.tb02125.x

By:

Beighton, P.;
Goldberg, L.;
Hof, J. Op't

Publication type:

Article

Is Menkes syndrome a copper storage disorder?

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 186, doi. 10.1111/j.1399-0004.1978.tb02128.x

By:

Horn, Nina;
Heydorn, K.;
Damsgaard, Else;
Tygstrup, Inge;
Vestermark, S.

Publication type:

Article

Journal of Immunogenetics.

Published in:: Clinical Genetics, 1978, v. 14, n. 3, p. 188, doi. 10.1111/j.1399-0004.1978.tb02129.x
Publication type:: Article

Prevalence of thyroid disorder in Down syndrome.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 154, doi. 10.1111/j.1399-0004.1978.tb02121.x

By:

ŠAre, Zlatko;
Ruvalcaba, R. H. A.;
Kelley, Vincent C.

Publication type:

Article

Partial trisomy 6.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 181, doi. 10.1111/j.1399-0004.1978.tb02127.x

By:

Fitch, Naomi

Publication type:

Article

The cloverleaf skull.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 178, doi. 10.1111/j.1399-0004.1978.tb02126.x

By:

Yujnovsky, Osvaldo;
Nyhan, Willlam L.

Publication type:

Article

Ultrasonography for guidance of amniocentesis in genetic counseling.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 133, doi. 10.1111/j.1399-0004.1978.tb02118.x

By:

Levine, Sandra C.;
Filly, Roy A.;
Golbus, Mitchell S.

Publication type:

Article

Partial tetrasomy 9 in a liveborn infant.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 147, doi. 10.1111/j.1399-0004.1978.tb02120.x

By:

Wisniewski, L.;
Politis, G. D.;
Higgins, J. V.

Publication type:

Article

Taurodontism and enamel hypomaturation associated with X-linked abnormalities.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 159, doi. 10.1111/j.1399-0004.1978.tb02122.x

By:

Gage, J. P.

Publication type:

Article

Ring chromosome 5 in two malformed boys with Cri du Chat syndrome.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 125, doi. 10.1111/j.1399-0004.1978.tb02116.x

By:

Suerinck, Eliane;
Noël, Bernard;
Rethore, Marie Odile

Publication type:

Article

Sex determination in nuclei of amnion fluid cells.

Published in:

Clinical Genetics, 1978, v. 14, n. 3, p. 169, doi. 10.1111/j.1399-0004.1978.tb02124.x

By:

Schwinger, E.;
Klimmeck, Doris;
Hansmann, M.

Publication type:

Article