Works matching IS 00099163 AND DT 1982 AND VI 22 AND IP 6

Results: 12

Trisomy 18 mosaicism: Clues to the diagnosis.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 327, doi. 10.1111/j.1399-0004.1982.tb01848.x

By:

Bass, Harold N.;
Fox, Michelle;
Wulfsberg, Eric;
Sparkes, Robert S.;
Crandall, BarbaraF

Publication type:

Article

Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocation.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 340, doi. 10.1111/j.1399-0004.1982.tb01850.x

By:

Pauli, Richard M.;
Kirkpatrick, Susan J.;
Meisner, Lorraine F.;
Mijanovich, James R.;
Spritz, Richard A.

Publication type:

Article

Metacarpophalangeal pattern profile analysis in Prader-WiIIi syndrome.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 315, doi. 10.1111/j.1399-0004.1982.tb01846.x

By:

Butler, Merlin G.;
Kaler, Stephen G.;
Yu, Pao-lo;
Meaney, F. John

Publication type:

Article

NADH dehydrogenase in cystic fibrosis.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 308, doi. 10.1111/j.1399-0004.1982.tb01844.x

By:

Sanguinetti-Briceno, Nelson R.;
Brock, David J. H.

Publication type:

Article

Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 348, doi. 10.1111/j.1399-0004.1982.tb01851.x

By:

Tomkins, Darrell J.;
Hunter, Alasdair G. w.;
Uchida, Irene A.;
Roberts, Maureen H.

Publication type:

Article

The Human Gene Map 20 October 1982.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 359, doi. 10.1111/j.1399-0004.1982.tb01853.x

By:

McKusick, Victor A.

Publication type:

Article

Genetic marker studies on a family with a 14/15 translocation.

Published in:: Clinical Genetics, 1982, v. 22, n. 6, p. 356, doi. 10.1111/j.1399-0004.1982.tb01852.x
Publication type:: Article

Congenital deafness and hypogonadism: a new X-linked recessive disorder.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 299, doi. 10.1111/j.1399-0004.1982.tb01843.x

By:

Myhre, S. A.;
Ruvalcaba, R. H. A.;
Kelley, V. C.

Publication type:

Article

Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 331, doi. 10.1111/j.1399-0004.1982.tb01849.x

By:

Kjellman, M.;
Laurell, A.-B.;
Löw, B.;
Sjöholm, A. G.

Publication type:

Article

Moebius syndrome in a child and extremity defect in her father.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 312, doi. 10.1111/j.1399-0004.1982.tb01845.x

By:

Collins, Debra L.;
Schimke, R. Neil

Publication type:

Article

Group-specific component (Gc) subtypes and schizophrenia.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 321, doi. 10.1111/j.1399-0004.1982.tb01847.x

By:

Papiha, S. S.;
Roberts, D. F.;
McLeish, L.

Publication type:

Article

Mosaic tetraploidy in a male neonate.

Published in:

Clinical Genetics, 1982, v. 22, n. 6, p. 295, doi. 10.1111/j.1399-0004.1982.tb01842.x

By:

Veenema, H.;
Tasseron, E. W. K.;
Geraedts, J. P. M.

Publication type:

Article