Works matching IS 00099163 AND DT 1982 AND VI 21 AND IP 2

Results: 12

Announcements.

Published in:: Clinical Genetics, 1982, v. 21, n. 2, p. 160, doi. 10.1111/j.1399-0004.1982.tb00753.x
Publication type:: Article

Holt-Oram syndrome: penetrance of the gene and lack of maternal effect.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 98, doi. 10.1111/j.1399-0004.1982.tb00743.x

By:

Gladstone, Igor;
Sybert, Virginia P.

Publication type:

Article

Serum cholinesterase in the mothers of neural tube defect progeny.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 130, doi. 10.1111/j.1399-0004.1982.tb00749.x

By:

Lawrie, S. S.;
Thomson, I.

Publication type:

Article

Treatment of phenylketonuria during pregnancy.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 141, doi. 10.1111/j.1399-0004.1982.tb00751.x

By:

Michels, Virginia V.;
Justice, Cynthia L.

Publication type:

Article

Partial trisomy 7p in two families resulting from different balanced translocations.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 112, doi. 10.1111/j.1399-0004.1982.tb00746.x

By:

Moore, C. M.;
Pfeiffer, R. A.;
Craig-Holmes, A. P.;
Scott, C. I.;
Meisel-Stosiek, M.

Publication type:

Article

Structural anomalies of the X chromosome: personal observation and review of non-mosaic cases.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 145, doi. 10.1111/j.1399-0004.1982.tb00752.x

By:

Wyss, Danielle;
DeLozier, Celia D.;
Daniell, James;
Engel, Eric

Publication type:

Article

Recurrence of the VATER association within a sibship.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 122, doi. 10.1111/j.1399-0004.1982.tb00747.x

By:

Auchterlonie, Ian A.;
White, Madeline P.

Publication type:

Article

Three distinct types of X-linked arthrogryposis seen in 6 families.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 81, doi. 10.1111/j.1399-0004.1982.tb00742.x

By:

Hall, J. G.;
Reed, S. D.;
Scott, C. I.;
Rogers, J. O.;
Jones, K. L.;
Camarano, A.

Publication type:

Article

Twins discordant for Down's syndrome.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 104, doi. 10.1111/j.1399-0004.1982.tb00744.x

By:

Benke, Paul J.

Publication type:

Article

Terminal deletion(4)(q33) in a male infant.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 125, doi. 10.1111/j.1399-0004.1982.tb00748.x

By:

Stamberg, Judith;
Jabs, Ethylin Wang;
Elias, Ellen

Publication type:

Article

Glycogen storage disease: long-term follow-up of nocturnal intragastric feeding.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 136, doi. 10.1111/j.1399-0004.1982.tb00750.x

By:

Michels, Virginia V.;
Beaudet, Arthur L.;
Potts, V. Elaine;
Montandon, Corinne M.

Publication type:

Article

Brachydactyly with major involvement of proximal phalanges.

Published in:

Clinical Genetics, 1982, v. 21, n. 2, p. 107, doi. 10.1111/j.1399-0004.1982.tb00745.x

By:

Fujimoto, Atsuko;
Smolensky, Louis S.;
Wilson, Miriam G.

Publication type:

Article