Works matching IS 00099163 AND DT 1990 AND VI 38 AND IP 3

Results: 11

Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 233, doi. 10.1111/j.1399-0004.1990.tb03575.x

By:

Reardon, William;
Temple, I. Karen;
Jones, Barry;
Baraitser, Michael

Publication type:

Article

An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 211, doi. 10.1111/j.1399-0004.1990.tb03572.x

By:

Leschot, N. J.;
Kanhai, H. H. H.;
Asperen, C. J.;
Wolf, H.;
Boer, K.;
Prooijen-Knegt, A. C.;
Christiaens, G. C. M. L.;
Verjaal, M.;
Briet, E.

Publication type:

Article

Activity of glucocerebrosidase in extracts of different cell types from type 1 Gaucher disease patients.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 218, doi. 10.1111/j.1399-0004.1990.tb03573.x

By:

Miranda, M. Clara Sa;
Aerts, Johannes M. F. G.;
Pinto, Rui;
Fontes, Augusta;
Lacerda, Lucia Wanzeller;
Weely, Sonja;
Barranger, John;
Tager, Joseph M.

Publication type:

Article

Friedreich's ataxia: a descriptive epidemiological study in an Italian population.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 161, doi. 10.1111/j.1399-0004.1990.tb03566.x

By:

Leone, Maurizio;
Brignolio, Francesco;
Rosso, Maria Gabriella;
Curtoni, Emilio Sergio;
Moroni, Antonio;
Tribolo, Antonella;
Schiffer, Davide

Publication type:

Article

Lacrimo-auriculo-dento-digital (LADD) syndrome with renal and foot anomalies.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 228, doi. 10.1111/j.1399-0004.1990.tb03574.x

By:

Roodhooft, A. M.;
Brussaard, C. C.;
Elst, E.;
Acker, K. J.

Publication type:

Article

Phenotypic variability in Meckel-Gruber syndrome.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 176, doi. 10.1111/j.1399-0004.1990.tb03568.x

By:

Farag, T. I.;
Usha, R.;
Uma, R.;
Mady, S. A.;
Al-Nagdy, K.;
El-Badramany, M. H.

Publication type:

Article

Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish families.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 187, doi. 10.1111/j.1399-0004.1990.tb03570.x

By:

Lehesjoki, Anna-Elina;
Rasi, Vesa;
Chapelle, Albert

Publication type:

Article

Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 198, doi. 10.1111/j.1399-0004.1990.tb03571.x

By:

Roskes, Erik J.;
Boughman, Joann A.;
Schwartz, Stuart;
Cohen, Maimon M.

Publication type:

Article

Familial caudal dysgenesis: evidence for a major dominant gene.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 170, doi. 10.1111/j.1399-0004.1990.tb03567.x

By:

Rudd, Noreen L.;
Klimek, Mary L.

Publication type:

Article

Letter to the Editors.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 237, doi. 10.1111/j.1399-0004.1990.tb03576.x

By:

Farag, Talaat I.;
Teebi, Ahmad S.

Publication type:

Article

Very early onset Huntington's disease: genetic mechanism and risk to siblings.

Published in:

Clinical Genetics, 1990, v. 38, n. 3, p. 180, doi. 10.1111/j.1399-0004.1990.tb03569.x

By:

Clarke, David J.;
Bundey, Sarah

Publication type:

Article