Works matching IS 00099163 AND DT 1990 AND VI 37 AND IP 5

Results: 11

Phenotype of two males with abnormal Y chromosomes.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 321, doi. 10.1111/j.1399-0004.1990.tb03513.x

By:

Mićić, M.;
Mićić, S.;
Babić, M.;
Diklić, V.

Publication type:

Article

Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 347, doi. 10.1111/j.1399-0004.1990.tb03517.x

By:

Legius, E.;
Fryns, J. P.;
Berghe, H.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1990, v. 37, n. 5, p. 416, doi. 10.1111/j.1399-0004.1990.tb03523.x
Publication type:: Article

X-linked myotubular myopathy: a linkage study.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 335, doi. 10.1111/j.1399-0004.1990.tb03515.x

By:

Darnfors, Catarina;
Larsson, H. E. Börje;
Oldfors, Anders;
Kyllerman, Mårten;
Gustavson, Karl-Henrik;
Bjursell, Gunnar;
Wahlström, Jan

Publication type:

Article

Consanguinity and confounding.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 415, doi. 10.1111/j.1399-0004.1990.tb03522.x

By:

Jeppesen, E. Z.;
Juul, S.

Publication type:

Article

The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 341, doi. 10.1111/j.1399-0004.1990.tb03516.x

By:

Borghgraef, M.;
Fryns, J. P.;
Berghe, H.

Publication type:

Article

Xbal polymorphism of the apolipoprotein B gene influences plasma lipid response to diet intervention.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 327, doi. 10.1111/j.1399-0004.1990.tb03514.x

By:

Tikkanen, M. J.;
Xu, C-F.;
Hämäläinen, T.;
Talmud, P.;
Sarna, S.;
Huttunen, J. K.;
Pietinen, P.;
Humphries, S.

Publication type:

Article

21st Symposium of the European Society of Human Genetics GENETICS IN CANCER & DEVELOPMENT Groningen May 11-13, 1989 Abstracts.

Published in:: Clinical Genetics, 1990, v. 37, n. 5, p. 367, doi. 10.1111/j.1399-0004.1990.tb03521.x
Publication type:: Article

How necessary is a chromosomal analysis in growth-retarded girls?

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 351, doi. 10.1111/j.1399-0004.1990.tb03518.x

By:

Eggert, P.;
Pankau, R.;
Oldigs, H. D.

Publication type:

Article

Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 355, doi. 10.1111/j.1399-0004.1990.tb03519.x

By:

Clarke, J. T. R.;
Willard, H. F.;
Teshima, I.;
Chang, P. L.;
Skomorowski, M. A.

Publication type:

Article

Trisomy 20q. A new case and further phenotypic delineation.

Published in:

Clinical Genetics, 1990, v. 37, n. 5, p. 363, doi. 10.1111/j.1399-0004.1990.tb03520.x

By:

Herens, C.;
Verloes, A.;
Laloux, F.;
Maldergem, L. Van

Publication type:

Article