Works matching IS 00099163 AND DT 1991 AND VI 40 AND IP 6

Results: 13

Cohen syndrome: fertility in a female patient.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 461, doi. 10.1111/j.1399-0004.1991.tb03118.x

By:

Fryns, J. P.;
Lemmens, F.;
Berghe, H.

Publication type:

Article

Chromosome aberrations in Sotos syndrome.

Published in:: Clinical Genetics, 1991, v. 40, n. 6, p. 472, doi. 10.1111/j.1399-0004.1991.tb03122.x
Publication type:: Article

Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 465, doi. 10.1111/j.1399-0004.1991.tb03119.x

By:

Friedrich, U.;
Larsen, T. B.;
Nielsen, J.

Publication type:

Article

Robertsonian translocations in Prader-Willi syndrome.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 471, doi. 10.1111/j.1399-0004.1991.tb03121.x

By:

Wenger, Sharon L.

Publication type:

Article

Genetic mapping of loci for X-linked retinitis pigmentosa.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 435, doi. 10.1111/j.1399-0004.1991.tb03115.x

By:

Dahl, N.;
Sundvall, M.;
Pettersson, U.;
Andréasson, S.;
Anvret, M.;
Kugelberg, U.;
Hagbyhn-Gericke, A.;
Goonewardena, P.

Publication type:

Article

De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 417, doi. 10.1111/j.1399-0004.1991.tb03112.x

By:

Schwartz, S.;
Harris, M.;
Ehrenpreis, R.;
Zaslav, A.;
Raffel, L. J.;
Schwartz, M. F.;
Lieber, E.;
Cohen, M. M.

Publication type:

Article

Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 430, doi. 10.1111/j.1399-0004.1991.tb03114.x

By:

Curfs, L. M. G.;
Wiegers, A. M.;
Sommers, J. R. M.;
Borghgraef, M.;
Fryns, J. P.

Publication type:

Article

Tests of performance of four semiautomatic metaphase-finding and karyotyping systems.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 441, doi. 10.1111/j.1399-0004.1991.tb03116.x

By:

Korthof, Gert;
Carothers, Andrew D.

Publication type:

Article

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 452, doi. 10.1111/j.1399-0004.1991.tb03117.x

By:

Sandgren, Ola;
Drugge, Ulf;
Holmgren, Gösta;
Sousa, Alda

Publication type:

Article

Simultaneous expression of the rare and common fragile sites on the X chromosome.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 423, doi. 10.1111/j.1399-0004.1991.tb03113.x

By:

Zaslav, Ann-Leslie;
Brown, W. Ted

Publication type:

Article

Erratum.

Published in:: Clinical Genetics, 1991, v. 40, n. 6, p. 474, doi. 10.1111/j.1399-0004.1991.tb03124.x
Publication type:: Article

An autosomal recessive form of benign familial neonatal seizures.

Published in:

Clinical Genetics, 1991, v. 40, n. 6, p. 467, doi. 10.1111/j.1399-0004.1991.tb03120.x

By:

Schiffmann, Raphael;
Shapira, Yehuda;
Ryan, Stephen G.

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1991, v. 40, n. 6, p. 473, doi. 10.1111/j.1399-0004.1991.tb03123.x
Publication type:: Article