Works matching IS 00099163 AND DT 1989 AND VI 35 AND IP 3

Results: 13

Tuberous sclerosis and the relation with renal angiomyolipoma. A genetic study on the clinical aspects.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 167, doi. 10.1111/j.1399-0004.1989.tb02924.x

By:

Baal, J. G.;
Fleury, P.;
Brummelkamp, W. H.

Publication type:

Article

6th International Congress on Cleft Palate and Related Craniofaclal Anomalies.

Published in:: Clinical Genetics, 1989, v. 35, n. 3, p. 232, doi. 10.1111/j.1399-0004.1989.tb02934.x
Publication type:: Article

21st Symposium of the European Society of Human Genetics, 'Genetics In Cancer & Development', Groningen, May 11-13, 1989.

Published in:: Clinical Genetics, 1989, v. 35, n. 3, p. 232, doi. 10.1111/j.1399-0004.1989.tb02933.x
Publication type:: Article

Fryns syndrome: report on 8 new cases.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 191, doi. 10.1111/j.1399-0004.1989.tb02927.x

By:

Aymé, S.;
Julian, C.;
Gambarelli, D.;
Mariotti, B.;
Luciani, A.;
Sudan, N.;
Maurin, N.;
Philip, N.;
Serville, F.;
Carles, D.;
Rolland, M.;
Giraud, F.

Publication type:

Article

Autosomal dominant inheritance in familial angiolipomatosis.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 202, doi. 10.1111/j.1399-0004.1989.tb02928.x

By:

Kumar, Ramesh;
Pereira, Brian J. G.;
Sakhuja, V.;
Chugh, K. S.

Publication type:

Article

Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 161, doi. 10.1111/j.1399-0004.1989.tb02923.x

By:

Chitayat, David;
Davis, Ellen B.;
McGillivray, Barbara C.;
Hayden, Michael R.;
Hall, Judith G.

Publication type:

Article

Prader-Willi syndrome and Sotos syndrome.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 228, doi. 10.1111/j.1399-0004.1989.tb02931.x

By:

Kennerknecht, I.

Publication type:

Article

Interstitial deletion of the long arm of chromosome 6(q22.2q23) in a boy with phenotypic features of Williams syndrome.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 230, doi. 10.1111/j.1399-0004.1989.tb02932.x

By:

Bzdúch, Vladimir;
Lukáčová, Margita

Publication type:

Article

3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 205, doi. 10.1111/j.1399-0004.1989.tb02929.x

By:

Verloes, A.;
Dresse, M.-F.;
Jovanovic, M.;
Dodinval, P.;
Geubelle, F.

Publication type:

Article

The Vth Nordic Meeting of Medical Genetics: Laugarvatn, Iceland, August 27-28, 1988.

Published in:: Clinical Genetics, 1989, v. 35, n. 3, p. 209, doi. 10.1111/j.1399-0004.1989.tb02930.x
Publication type:: Article

Genetics Short Course.

Published in:: Clinical Genetics, 1989, v. 35, n. 3, p. 232, doi. 10.1111/j.1399-0004.1989.tb02935.x
Publication type:: Article

Phenotypical features of an unique Irish family with severe autosomal recessive Osteogenesis imperfecta.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 181, doi. 10.1111/j.1399-0004.1989.tb02926.x

By:

Williams, E. Mair;
Nicholls, Alan C.;
Daw, Sara C. M.;
Mitchell, Nan;
Levin, L. Stefan;
Green, Bryan;
MacKenzie, Janet;
Evans, Dewi-R.;
Chudleigh, Patricia A.;
Pope, F. Michael

Publication type:

Article

Chorionic villi sampling for early prenatal diagnosis: an option for the Jewish orthodox community.

Published in:

Clinical Genetics, 1989, v. 35, n. 3, p. 174, doi. 10.1111/j.1399-0004.1989.tb02925.x

By:

Zakut, H.;
Zamir, R.;
Yemini, O.;
Sindel, L.;
Kohn, G.

Publication type:

Article