Works matching IS 00099163 AND DT 1981 AND VI 19 AND IP 3

Results: 14

Prenatal diagnosis of campomelic dwarfism.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 199, doi. 10.1111/j.1399-0004.1981.tb00696.x

By:

Fryns, J. P.;
Berghe, K. van den;
Assche, A. van;
Berghe, H. van den

Publication type:

Article

Klinefelter's syndrome with a 47, XXY, inv (12) (q15q24) karyotype.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 188, doi. 10.1111/j.1399-0004.1981.tb00694.x

By:

Singh, Roderick P.

Publication type:

Article

HLA profile and Reiter's syndrome.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 159, doi. 10.1111/j.1399-0004.1981.tb00690.x

By:

Schultz, Jane S.;
Good, Armin E.;
Sing, Charles F.;
Kapur, Janet J.

Publication type:

Article

Trisomy 6qter.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 202, doi. 10.1111/j.1399-0004.1981.tb00697.x

By:

Turleau, C.;
Grouchy, J. de

Publication type:

Article

Increased frequencies of chromosomal abnormalities in families with a history of fetal wastage.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 168, doi. 10.1111/j.1399-0004.1981.tb00691.x

By:

Nordenson, Ingrid

Publication type:

Article

Letter to the Editors.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 209, doi. 10.1111/j.1399-0004.1981.tb00699.x

By:

Hall, Judith G.;
Hauck, Robert C.

Publication type:

Article

An XXXY boy with X/XY half-sister.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 181, doi. 10.1111/j.1399-0004.1981.tb00693.x

By:

Welch, Michael J.;
Sparkes, Robert S.

Publication type:

Article

Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 174, doi. 10.1111/j.1399-0004.1981.tb00692.x

By:

Silengo, Margherita Cirillo;
Luzzatti, Luigi;
Centerwall, Willard R.;
Costello, Jack M.;
Parslow, Malcolm

Publication type:

Article

Variation in nucleolar organizer activity in lymphocytes of females with adenocarcinoma.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 145, doi. 10.1111/j.1399-0004.1981.tb00687.x

By:

Cheng, D. M.;
Denton, T. E.;
Liem, S. L.;
Elliot, C. L.

Publication type:

Article

Pregnancy in Bloom's Syndrome.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 156, doi. 10.1111/j.1399-0004.1981.tb00689.x

By:

Mulcahy, Marie T.;
French, Martyn

Publication type:

Article

Familial tricho-rhino-phalangeal syndrome Type II.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 149, doi. 10.1111/j.1399-0004.1981.tb00688.x

By:

Murachi, S.;
Nogami, H.;
Oki, T.;
Ogino, T.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1981, v. 19, n. 3, p. 210, doi. 10.1111/j.1399-0004.1981.tb00700.x
Publication type:: Article

Orbital cyst in addition to congenital cerebral and focal dermal malformations: A new entity?

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 191, doi. 10.1111/j.1399-0004.1981.tb00695.x

By:

Delleman, J. W.;
Oorthuys, J. W. E.

Publication type:

Article

Normal Hageman factor level in 7q deletion syndrome.

Published in:

Clinical Genetics, 1981, v. 19, n. 3, p. 207, doi. 10.1111/j.1399-0004.1981.tb00698.x

By:

Kawashima, Hiroko;
Taniguchi, Noboru

Publication type:

Article