Works matching IS 00099163 AND DT 1983 AND VI 24 AND IP 6

Results: 14

Linkage analysis in von Willebrand disease.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 434, doi. 10.1111/j.1399-0004.1983.tb00099.x

By:

Verp, M. S.;
Radvany, R. M.;
Green, D.;
Conneally, P. M.;
Patel, V. A.;
Martin, A. O.;
Simpson, J. L.

Publication type:

Article

Prader-Willi syndrome associated with inversion of chromosome 15.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 456, doi. 10.1111/j.1399-0004.1983.tb00104.x

By:

Winsor, Elizabeth J. T.;
Welch, J. Philip

Publication type:

Article

Fragile X syndrome in mildly mentally retarded children in a Northern Swedish county. A prevalence study.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 393, doi. 10.1111/j.1399-0004.1983.tb00092.x

By:

Blomquist, H. K:son;
Gustavson, K-H.;
Holmgren, G.;
Nordenson, I.;
Pålsson-Stråe, U.

Publication type:

Article

The femur, fibula, ulna (FFU) complex in siblings.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 449, doi. 10.1111/j.1399-0004.1983.tb00102.x

By:

Zlotogora, J.;
Rosenmann, E.;
Menashe, M.;
Robin, G. C.;
Cohen, T.

Publication type:

Article

Letter to the Editors.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 462, doi. 10.1111/j.1399-0004.1983.tb00105.x

By:

Powell, Frank C.;
Winkelmann, Richard K.;
Gordon, Hymie

Publication type:

Article

Genetic regulation of the red cell uroporphyrinogen-l-synthetase level in families with acute intermittent porphyria.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 403, doi. 10.1111/j.1399-0004.1983.tb00094.x

By:

Wetterberg, L.;
Floderus, Y.;
Thunell, S.;
Iselius, L.;
Lindsten, J.

Publication type:

Article

Additional data on spontaneous abortion and facial cleft malformations.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 407, doi. 10.1111/j.1399-0004.1983.tb00095.x

By:

Bear, J. C.

Publication type:

Article

The relevance of pre-amniocentesis pedigree analysis and genetic counseling.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 429, doi. 10.1111/j.1399-0004.1983.tb00098.x

By:

Holzgreve, Brigitte;
Holzgreve, Wolfgang;
Golbus, Mitchell S.

Publication type:

Article

Genetic regulation of melatonin excretion in urine.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 399, doi. 10.1111/j.1399-0004.1983.tb00093.x

By:

Wetterberg, Lennart;
Iselius, Lennart;
Lindsten, Jan

Publication type:

Article

Association between the degree of mosaicism and the severity of syndrome in Turner mosaics and Klinefelter mosaics.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 420, doi. 10.1111/j.1399-0004.1983.tb00097.x

By:

Sarkar, Rita;
Marimuthu, K. M.

Publication type:

Article

Y chromosome length related to fetal loss.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 413, doi. 10.1111/j.1399-0004.1983.tb00096.x

By:

Westlake, J. R.;
Robertson, R.;
Leddet, I.;
Funderburk, S. J.;
Sparkes, R. S.

Publication type:

Article

Silver-Russell syndrome with absence of digits and syndactylism of the fingers.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 453, doi. 10.1111/j.1399-0004.1983.tb00103.x

By:

Keppen, Laura Davis;
Rennert, Owen M.

Publication type:

Article

Male to male transmission of the G syndrome.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 446, doi. 10.1111/j.1399-0004.1983.tb00101.x

By:

Farndon, Peter A.;
Donnai, Dian

Publication type:

Article

The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.

Published in:

Clinical Genetics, 1983, v. 24, n. 6, p. 439, doi. 10.1111/j.1399-0004.1983.tb00100.x

By:

VOOREN, M. J. VAN DE;
NIERMEIJER, M. F.;
HOOGEBOOM, A. J. M.

Publication type:

Article