Works matching IS 00099163 AND DT 1987 AND VI 31 AND IP 1

Results: 12

Triphalangeal thumb and brachy-ectrodactyly syndrome.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 13, doi. 10.1111/j.1399-0004.1987.tb02761.x

By:

Silengo, M. Cirillo;
Biagioli, M.;
Bell, G. Lopez;
Bona, G.;
Franceschini, P.

Publication type:

Article

Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 53, doi. 10.1111/j.1399-0004.1987.tb02767.x

By:

Tengstrqm, Carola;
Autto, Seppo

Publication type:

Article

Trends in European Multiple Sclerosis Research Lyon, France September 3-5, 1987.

Published in:: Clinical Genetics, 1987, v. 31, n. 1, p. 64, doi. 10.1111/j.1399-0004.1987.tb02770.x
Publication type:: Article

Bloom's syndrome with porokeratosis of Mibeili and multiple cancers of the skin, lung and colon.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 35, doi. 10.1111/j.1399-0004.1987.tb02764.x

By:

Takemiya, Masataka;
Shiraishi, Satoshi;
Teramoto, Tatsuyuki;
Miki, Yoshiharu

Publication type:

Article

Prenatal diagnosis in Becker muscular dystrophy.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 45, doi. 10.1111/j.1399-0004.1987.tb02765.x

By:

Wood, Stephen;
Shukin, Robert J.;
Yong, Siu Li;
Wilson, Doug;
Kalousek, Dagmar;
Chudley, Albert

Publication type:

Article

'Unclassifiable' weak A blood group and deficient H phenotype (Hm) in one pedigree.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 7, doi. 10.1111/j.1399-0004.1987.tb02760.x

By:

Light, Jan;
Wenk, Robert E.;
Greenwell, Pamela

Publication type:

Article

Carrier Detection in DMD.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 62, doi. 10.1111/j.1399-0004.1987.tb02769.x

By:

Uppal, Gurjeet;
Dewbury, K. C.;
Dennis, N. R.

Publication type:

Article

A male infant with holoprosencephaly, associated with ring chromosome 21.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 48, doi. 10.1111/j.1399-0004.1987.tb02766.x

By:

Aronson, D. C.;
Jansweijer, M. C. E.;
Hoovers, J. M. N.;
Barth, P. G.

Publication type:

Article

Heterozygous manifestations of Langer mesomelic dysplasia.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 19, doi. 10.1111/j.1399-0004.1987.tb02762.x

By:

Goldblatt, J.;
Wallis, C.;
Vilioen, D.;
Beighton, P.

Publication type:

Article

Population cytogenetics of autosomal fragile sites.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 61, doi. 10.1111/j.1399-0004.1987.tb02768.x

By:

Fryns, J. P.;
Petit, P.

Publication type:

Article

In vitro hyperdiploidy in dermal fibroblasts: evidence for genetic predisposition in aerodigestive tract cancer.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 25, doi. 10.1111/j.1399-0004.1987.tb02763.x

By:

Danes, B. Shannon;
Boyle, Paula D.;
Traganos, Frank.;
Ringborg, Ulrik;
Melamed, Myron R.

Publication type:

Article

Fragile 19p13 in a family with mental illness.

Published in:

Clinical Genetics, 1987, v. 31, n. 1, p. 1, doi. 10.1111/j.1399-0004.1987.tb02759.x

By:

Chodirker, B. N.;
Chudley, A. E.;
Ray, M.;
Wickstrom, D. E.;
Riordan, D. L.

Publication type:

Article