Works matching IS 00099163 AND DT 1989 AND VI 35 AND IP 4

Results: 15

Trisomy 5 mosaicism in amniotic fluid with normal outcome.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 282, doi. 10.1111/j.1399-0004.1989.tb02944.x

By:

Casamassima, Anthony C.;
Wilmot, Patrick L.;
Mahoney, Maurice J.;
Scott, Robin V.;
Shapiro, Lawrence R.

Publication type:

Article

Trisomy 9q3 syndrome: a case report and review of the literature.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 293, doi. 10.1111/j.1399-0004.1989.tb02947.x

By:

Naritomi, K.;
Izumikawa, Y.;
Goya, Y.;
Gushiken, M.;
Shiroma, N.;
Hirayama, K.

Publication type:

Article

On the familial occurrence of congenital bilateral absence of vas deferens.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 268, doi. 10.1111/j.1399-0004.1989.tb02941.x

By:

Kleczkowska, A.;
Fryns, J. P.;
Steeno, O.;
Berghe, H.

Publication type:

Article

Nonsyndromal microphthalmia.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 311, doi. 10.1111/j.1399-0004.1989.tb02950.x

By:

Teebi, Ahmad S.;
Al-Saleh, Qusay A.

Publication type:

Article

A 45,X/69,XXY fetus.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 285, doi. 10.1111/j.1399-0004.1989.tb02945.x

By:

Betts, David R.;
Fear, Claudine N.;
Barby, Teresa;
Seller, Mary J.

Publication type:

Article

A new case of deletion 1q42 syndrome.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 289, doi. 10.1111/j.1399-0004.1989.tb02946.x

By:

Tolkendorf, E.;
Hinkel, G. K.;
Gabriel, A.

Publication type:

Article

Dermatoglyphic features of a male with diploid/tetraploid mosaicism.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 310, doi. 10.1111/j.1399-0004.1989.tb02949.x

By:

Wittwer, B. Bernhard;
Wittwer, H. Bärbel

Publication type:

Article

Molecular deletions in the Duchenne/Becker muscular dystrophy gene.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 251, doi. 10.1111/j.1399-0004.1989.tb02939.x

By:

Hart, Kevin A.;
Abbs, Stephen;
Wapenaar, Martin C.;
Cole, Charlotte G.;
Hodgson, Shirley V.;
Bobrow, Martin

Publication type:

Article

Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 233, doi. 10.1111/j.1399-0004.1989.tb02936.x

By:

Myers, T. L.;
Prouty, L. A.

Publication type:

Article

Two other cases of ANOTHER syndrome? Family report and update.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 237, doi. 10.1111/j.1399-0004.1989.tb02937.x

By:

Pinheiro, Marta;
Penna, Francisco José;
Freire-Maia, N.

Publication type:

Article

Prader-Willi Syndrome Scientific Conference III Abstracts.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 299, doi. 10.1111/j.1399-0004.1989.tb02948.x

By:

Hall, Bryan D.

Publication type:

Article

Brachydactyly type A-7 (Smorgasbord): a new entity.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 261, doi. 10.1111/j.1399-0004.1989.tb02940.x

By:

Meiselman, Samuel A.;
Berkenstadt, Michal;
Ben-Ami, Tami;
Goodman, Richard M.

Publication type:

Article

Sjögren-Larsson syndrome in Sweden: distribution of the gene.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 272, doi. 10.1111/j.1399-0004.1989.tb02942.x

By:

Iselius, L.;
Jagell, S.

Publication type:

Article

Variant nucleolus organizing regions and the risk of Down syndrome.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 243, doi. 10.1111/j.1399-0004.1989.tb02938.x

By:

Green, Jeffrey E.;
Rosenbaum, Kenneth N.;
Rapoport, Stanley I.;
Schapiro, Mark B.;
White, Beverly J.

Publication type:

Article

An interstitial deletion of the long arm of chromosome 13.

Published in:

Clinical Genetics, 1989, v. 35, n. 4, p. 276, doi. 10.1111/j.1399-0004.1989.tb02943.x

By:

Roland, B.;
Lowry, R. B.;
Robertson, A. S.;
Cox, D. M.

Publication type:

Article