Works matching IS 00099163 AND DT 1992 AND VI 41 AND IP 3

Results: 11

Monosomy 6q: report on four new cases.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 159, doi. 10.1111/j.1399-0004.1992.tb03655.x

By:

Valtat, C.;
Galliano, D.;
Mettey, R.;
Toutain, A.;
Moraine, C.

Publication type:

Article

A new chromosome 9 variant: an extra band within the 9qh region.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 157, doi. 10.1111/j.1399-0004.1992.tb03654.x

By:

Hoo, Joe J.

Publication type:

Article

Experiences with risk estimates for carriers of chromosomal reciprocal translocations.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 113, doi. 10.1111/j.1399-0004.1992.tb03646.x

By:

Midro, Alina T.;
Stengel-Rutkowski, Sabine;
Stene, Jon

Publication type:

Article

Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 135, doi. 10.1111/j.1399-0004.1992.tb03649.x

By:

Bergan, A. A. B.;
Schuurman, L J. M.;
Born, L. I.;
Samanns, G.;
Dorp, D. B.;
Pinckers, A. J. L. G.;
Bakker, E.;
Ommen, G. J. B.;
Gal, A.;
Bleeker-Wagemakers, E. M.

Publication type:

Article

The trichorhinophalangeal syndrome with repeated dislocation of the patella.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 139, doi. 10.1111/j.1399-0004.1992.tb03650.x

By:

Puliyel, Jacob M.;
Puliyel, Matthew M.;
Varughese, Sara

Publication type:

Article

Influence of apolipoprotein B signal peptide insertion/deletion polymorphism on serum lipids and apolipoproteins in a Chinese population.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 152, doi. 10.1111/j.1399-0004.1992.tb03653.x

By:

Saha, N.;
Tay, J. S. H.;
Chew, L. S.

Publication type:

Article

Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 alleles.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 123, doi. 10.1111/j.1399-0004.1992.tb03647.x

By:

Kalaydjieva, L.;
Dworniczak, B.;
Kromensky, I.;
Koprivarova, K.;
Radeva, B.;
Milusheva, R.;
Aulehla-Scholz, C.;
Horst, J.

Publication type:

Article

Nonrandom chromosome breakpoints in 6q deletions.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 167, doi. 10.1111/j.1399-0004.1992.tb03656.x

By:

Hecht, Frederick;
Hecht, Barbara K.

Publication type:

Article

Partial trisomy 19p: case report and natural history.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 143, doi. 10.1111/j.1399-0004.1992.tb03651.x

By:

Salbert, B. A.;
Solomon, M.;
Spence, J. L.;
Jackson-Cook, C.;
Brown, J.;
Bodurtha, J.

Publication type:

Article

Karyotype/phenotype correlation in females with short stature.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 147, doi. 10.1111/j.1399-0004.1992.tb03652.x

By:

Temtamy, Samia A.;
Ghali, Isis;
Salam, Mouchira A.;
Hussein, Fawzia H.;
Ezz, Eman H. A. Aboul;
Salah, Nermin

Publication type:

Article

Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita.

Published in:

Clinical Genetics, 1992, v. 41, n. 3, p. 129, doi. 10.1111/j.1399-0004.1992.tb03648.x

By:

Kehrer, Hildegard;
Krone, Winfrid;
Schindler, Oetlav;
Kaufmann, Roland;
Schrezenmeler, Hubert

Publication type:

Article