Works matching IS 00099163 AND DT 1985 AND VI 28 AND IP 3

Results: 14

The size of prometaphase chromosome segments Tables using percentages of haploid autosome length (750 band stage.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 216, doi. 10.1111/j.1399-0004.1985.tb00389.x

By:

Daniel, Art

Publication type:

Article

X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritance.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 238, doi. 10.1111/j.1399-0004.1985.tb00392.x

By:

Wieacker, Peter;
Zimmer, Jürgen;
Ropers, Hans-Hilger

Publication type:

Article

Cortical blindness, growth and psychomotor retardation and postaxial Polydactyly: A probably distinct autosomal recessive syndrome.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 251, doi. 10.1111/j.1399-0004.1985.tb00395.x

By:

Hernández, Alejandro;
García-Esquivel, Lidia;
Reynoso, Martha Celina;
Fragoso, Rubén;
Enríquez-Guerra, Miguel Angel;
Nazará, Zamira;
Anzar, Miguel Bracamontes;
Cantú, José María

Publication type:

Article

Maternal cell contamination in chorionic villi cultures - Exclusion by chromosomal fluorescence polymorphisms.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 262, doi. 10.1111/j.1399-0004.1985.tb00398.x

By:

Miny, Peter;
Holzgreve, Wolfgang;
Basaran, Seher;
Gerbaulet, Karl-Hermann;
Beller, Fritz K.;
Pawlowitzki, Ivar-Harry

Publication type:

Article

A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 255, doi. 10.1111/j.1399-0004.1985.tb00396.x

By:

Stoll, C.;
Talon, P.;
Mengus, L.;
Roth, M. P.;
Dott, B.

Publication type:

Article

Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathy.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 185, doi. 10.1111/j.1399-0004.1985.tb00386.x

By:

Lin, Henry J.;
Rotter, Jerome I.;
Conte, William J.

Publication type:

Article

Sotos syndrome - autosomal dominant inheritance substantiated.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 243, doi. 10.1111/j.1399-0004.1985.tb00393.x

By:

Winship, Ingrid M.

Publication type:

Article

Agenesis of the corpus callosum and macrocephaly in siblings.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 225, doi. 10.1111/j.1399-0004.1985.tb00390.x

By:

Young, I. D.;
Trounce, J. Q.;
Levene, M. I.;
Fitzsimmons, J. S.;
Moore, J. R.

Publication type:

Article

I-cell disease: clinical studies of 21 Japanese cases.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 207, doi. 10.1111/j.1399-0004.1985.tb00388.x

By:

Okada, Shintaro;
Owada, Misao;
Sakiyama, Takeshi;
Yutaka, Tohru;
Ogawa, Minoru

Publication type:

Article

Trismus-pseudocamptodactyly syndrome in a Japanese family.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 247, doi. 10.1111/j.1399-0004.1985.tb00394.x

By:

Tsukahara, M.;
Shinozaki, F.;
Kajii, T.

Publication type:

Article

Direct and maternal aspects of the risk of cataract with partial disorders of galactose metabolism.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 199, doi. 10.1111/j.1399-0004.1985.tb00387.x

By:

Winder, A. F.;
Fielder, A. R.;
Mount, J. N.;
Menzies, J. S.

Publication type:

Article

A test of a climate room for preparation of chromosome slides.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 260, doi. 10.1111/j.1399-0004.1985.tb00397.x

By:

Lundsteen, Claes;
Lind, Anne-Marie

Publication type:

Article

Steroid sulphatase deficiency disease.

Published in:

Clinical Genetics, 1985, v. 28, n. 3, p. 231, doi. 10.1111/j.1399-0004.1985.tb00391.x

By:

Lykkesfeldt, Gert;
Høyer, Henrik;
Ibsen, Hans Henning;
Brandrup, Flemming

Publication type:

Article

ERRATUM.

Published in:: Clinical Genetics, 1985, v. 28, n. 3, p. 264, doi. 10.1111/j.1399-0004.1985.tb00399.x
Publication type:: Article