Works matching IS 00099163 AND DT 1987 AND VI 32 AND IP 3

Results: 15

The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 160, doi. 10.1111/j.1399-0004.1987.tb03347.x

By:

Schinzel, Albert

Publication type:

Article

Three-generation transmission of Hirschsprung's disease.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 175, doi. 10.1111/j.1399-0004.1987.tb03350.x

By:

Lipson, A. H.;
Harvey, J.

Publication type:

Article

Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 179, doi. 10.1111/j.1399-0004.1987.tb03351.x

By:

Borghgraef, M.;
Fryns, J. P.;
Dlelkens, A.;
Pyck, K.;
Berghe, H. Van Den

Publication type:

Article

X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 192, doi. 10.1111/j.1399-0004.1987.tb03353.x

By:

Alitalo, Tiina;
Kärnä, Jussi;
Forsius, Henjik;
Chapelle, Albert

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1987, v. 32, n. 3, p. 208, doi. 10.1111/j.1399-0004.1987.tb03358.x
Publication type:: Article

Familial absence of the trapezius muscle with associated shoulder girdle abnormalities.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 145, doi. 10.1111/j.1399-0004.1987.tb03344.x

By:

Gross-Kieselstein, E.;
Shalev, R. S.

Publication type:

Article

Clinical anophthalmos in a family.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 156, doi. 10.1111/j.1399-0004.1987.tb03346.x

By:

Sensi, A.;
Incorvaia, C.;
Sebastiani, A.;
Calzolari, E.

Publication type:

Article

Ehlers-Danlos syndrome: yet another type?

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 196, doi. 10.1111/j.1399-0004.1987.tb03354.x

By:

Viljoen, Denis;
Goldblatt, Jack;
Thompson, Dave;
Beighton, Peter

Publication type:

Article

Holoprosencephaly associated with ring chromosome 21.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 207, doi. 10.1111/j.1399-0004.1987.tb03357.x

By:

Hoovers, J. M. N.;
Jansweijer, M. C. E.

Publication type:

Article

Severity and recurrence risk of congenital heart defects exemplified by atrial septal defect secundum.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 148, doi. 10.1111/j.1399-0004.1987.tb03345.x

By:

Gold, R. J. M.;
Rose, V.;
Yau, Y.

Publication type:

Article

Postaxial polydactyly in association with neurofibromatosis.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 202, doi. 10.1111/j.1399-0004.1987.tb03355.x

By:

Merlob, Paul;
Levy, Yizhak;
Shuper, Avinoam

Publication type:

Article

Ichthyosis-cheek-eyebrow syndrome (ICE(.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 206, doi. 10.1111/j.1399-0004.1987.tb03356.x

By:

Goodman, R. M.;
Sidransky, E.;
Feinstein, A.

Publication type:

Article

Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein?

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 172, doi. 10.1111/j.1399-0004.1987.tb03349.x

By:

Petit, P.;
Bossens, M.;
Thomas, D.;
Moerman, Ph;
Fryns, J. P.;
Berghe, H.

Publication type:

Article

Evidence for a sperm mutation resulting in Duchenne muscular dystrophy.

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 187, doi. 10.1111/j.1399-0004.1987.tb03352.x

By:

Børresen, A. L.;
Heiberg, A.;
Møller, P.;
Berg, K.

Publication type:

Article

Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(P25;q24).

Published in:

Clinical Genetics, 1987, v. 32, n. 3, p. 169, doi. 10.1111/j.1399-0004.1987.tb03348.x

By:

Kristoffersson, Ulf;
Heim, Sverre;
Mandahl, Nils;
Sundkvist, Lennart;
Szelest, Jan;
Hägerstrand, Inga

Publication type:

Article