Works matching IS 00099163 AND DT 1987 AND VI 32 AND IP 2

Results: 14

Effect of combinations of antioxidants on oxygen radical-induced sister chromatid exchanges.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 114, doi. 10.1111/j.1399-0004.1987.tb03336.x

By:

Weitberg, Alan B.

Publication type:

Article

Major locus for red hair color linked to MNS blood groups on chromosome 4.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 125, doi. 10.1111/j.1399-0004.1987.tb03339.x

By:

Eiberg, Hans;
Mohr, Jan

Publication type:

Article

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 118, doi. 10.1111/j.1399-0004.1987.tb03337.x

By:

Bisgaard, M. L.;
Eiberg, H.;
Møller, N.;
Niebuhr, E.;
Mohr, J.

Publication type:

Article

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 129, doi. 10.1111/j.1399-0004.1987.tb03340.x

By:

Eiberg, H.;
Bixler, D.;
Nielsen, L. S.;
Conneally, P. M.;
Mohr, J.

Publication type:

Article

X-linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous female.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 95, doi. 10.1111/j.1399-0004.1987.tb03332.x

By:

Keppen, Laura Davis;
Husain, Muhammad M.;
Woody, Robert C.

Publication type:

Article

Microcephalic osteodysplastic dwarfism (Type ll-like) in siblings.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 88, doi. 10.1111/j.1399-0004.1987.tb03331.x

By:

Verloes, Alain;
Lambrechts, Lucien;
Senterre, Jacques;
Lambotte, Claude

Publication type:

Article

Hereditary hypotrichosis simplex of the scalp.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 120, doi. 10.1111/j.1399-0004.1987.tb03338.x

By:

Kohn, Gertrude;
Metzker, Aryeh

Publication type:

Article

Incidence of familial dysautonomia in Israel 1977-1981.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 106, doi. 10.1111/j.1399-0004.1987.tb03334.x

By:

Maayan, Ch.;
Kaplan, E.;
Shachar, Sh.;
Peleg, O.;
Godfrey, S.

Publication type:

Article

Inverted tandem duplication generates a duplication deficiency of chromosome 8p.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 109, doi. 10.1111/j.1399-0004.1987.tb03335.x

By:

Dill, F. J.;
Schertzer, M.;
Sandercock, J.;
Tischler, B.;
Wood, S.

Publication type:

Article

A case of first trimester chromosomal mosaicism confined to the cultivation of the gestational products.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 133, doi. 10.1111/j.1399-0004.1987.tb03341.x

By:

Smidt-Jensen, Steen;
Lind, Anne-Marie

Publication type:

Article

Heterogeneity of pseudoxanthoma elasticum: delineation of a new form?

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 100, doi. 10.1111/j.1399-0004.1987.tb03333.x

By:

Viljoen, D. L.;
Pope, F. M.;
Beighton, P.

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1987, v. 32, n. 2, p. 144, doi. 10.1111/j.1399-0004.1987.tb03343.x
Publication type:: Article

Partial trisomy 3q syndrome inherited from familal t(3;9) (q26.1;p23).

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 137, doi. 10.1111/j.1399-0004.1987.tb03342.x

By:

Tranebjærg, Lisbeth;
Bækmark, Ulla Britt;
Dyhr-Nœlsen, Margrethe;
Kreiborg, Sven

Publication type:

Article

Chromosome studies in IgA-deficient patients.

Published in:

Clinical Genetics, 1987, v. 32, n. 2, p. 81, doi. 10.1111/j.1399-0004.1987.tb03330.x

By:

Taalman, R. D. F. M.;
Weemaes, C. M. R.;
Hustinx, T. W. J.;
Scheres, J. M. J. C.;
Clement, J. M. E.;
Stoelinga, G. B. A.

Publication type:

Article