Works matching IS 00099163 AND DT 1980 AND VI 18 AND IP 5

Results: 11

Partial trisomy 1 (q42→ter).

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 371, doi. 10.1111/j.1399-0004.1980.tb02297.x

By:

Leisti, J.;
Aula, P.

Publication type:

Article

A and B Postaxial polydactyly in two members of the same family.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 342, doi. 10.1111/j.1399-0004.1980.tb02294.x

By:

Ventruto, V.;
Theo, G.;
Celona, A.;
Fioretti, G.;
Pagano, L.;
Stabile, M.;
Cavaliere, M. L.

Publication type:

Article

Familial pterygium syndrome.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 317, doi. 10.1111/j.1399-0004.1980.tb02291.x

By:

Stoll, C.;
Levy, J.-M.;
Kehr, P.;
Roth, M.-P.

Publication type:

Article

Somatic cell genetic studies of the cystic fibrosis mucociliary inhibitor.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 379, doi. 10.1111/j.1399-0004.1980.tb02298.x

By:

Mayo, Brenda J.;
Klebe, Robert J.;
Barnett, Don R.;
Lankford, B. J.;
Bowman, Barbara H.

Publication type:

Article

Partial trisomy 21.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 392, doi. 10.1111/j.1399-0004.1980.tb02300.x

By:

Pueschel, Siegfried M.;
Padre-Mendoza, Teresita;
Ellenbogen, Richard

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1980, v. 18, n. 5, p. 396, doi. 10.1111/j.1399-0004.1980.tb02301.x
Publication type:: Article

Two patients with an unusual form of type II fucosidosis.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 348, doi. 10.1111/j.1399-0004.1980.tb02295.x

By:

Schoonderwaldt, H. C.;
Lamers, K. J. B.;
Kleijnen, F. M.;
Berg, C. J. M. G.;
Bruyn, C. H. M. M.

Publication type:

Article

Quantitative analysis of 6985 digitized trypsin G -banded human metaphase chromosomes.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 355, doi. 10.1111/j.1399-0004.1980.tb02296.x

By:

Lundsieen, Claes;
Philip, John;
Granum, Erik

Publication type:

Article

Intrafamilial associations of cholesterol and triglyceride among related and unrelated household members.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 321, doi. 10.1111/j.1399-0004.1980.tb02292.x

By:

Morrison, John A.;
Laskarzewski, Peter M.;
Khoury, Philip;
Samuels, Steven J.;
Kelly, Kathy K.;
Mellies, Margot J.;
Glueck, Charles. J.

Publication type:

Article

Lymph vessel defects in patients with ovarian dysgenesis.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 387, doi. 10.1111/j.1399-0004.1980.tb02299.x

By:

Vittay, P.;
Bösze, P.;
Gaál, Magdolna;
László, J.

Publication type:

Article

Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation.

Published in:

Clinical Genetics, 1980, v. 18, n. 5, p. 329, doi. 10.1111/j.1399-0004.1980.tb02293.x

By:

Caskey, C. Thomas;
Nussbaum, Robert L.;
Cohan, Leslie C.;
Pollack, Lynda

Publication type:

Article