Works matching IS 00099163 AND DT 1989 AND VI 36 AND IP 1

Results: 14

A familial chromosomal translocation t(6q;7q) with habitual abortions.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 1, doi. 10.1111/j.1399-0004.1989.tb03359.x

By:

Zhang, Sizhong;
Wu, Xiaoyan;
Ho, Qun;
Zhao, Li

Publication type:

Article

X-linked myotubular myopathy: clinical and pathological findings in a family.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 5, doi. 10.1111/j.1399-0004.1989.tb03360.x

By:

Oldfors, A.;
Kyllerman, M.;
Wahlström, J.;
Darnfors, C.;
Henriksson, K. G.

Publication type:

Article

A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 31, doi. 10.1111/j.1399-0004.1989.tb03363.x

By:

Norman, Andrew;
Harper, Peter

Publication type:

Article

An aetiological study of isochromosome-X Turner's syndrome.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 53, doi. 10.1111/j.1399-0004.1989.tb03366.x

By:

Carothers, Andrew D.;
Mey, Rhona De;
Daker, Michael;
Boyd, Elizabeth;
Connor, Michael;
Ellis, Patricia M.;
Stevenson, David

Publication type:

Article

Trisomy 1q.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 75, doi. 10.1111/j.1399-0004.1989.tb03371.x

By:

Kiss, P.;
Imrei, Júlia

Publication type:

Article

Leukocyte and plasma N-laurylsphingosine deacylase (ceramidase) in Farber disease.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 38, doi. 10.1111/j.1399-0004.1989.tb03364.x

By:

Ben-Yoseph, Y.;
Gagné, R.;
Parvathy, M. R.;
Mitchell, D. A.;
Momoi, T.

Publication type:

Article

Aarskog syndrome in Hungary.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 73, doi. 10.1111/j.1399-0004.1989.tb03370.x

By:

Kiss, P.

Publication type:

Article

Perception of burden among at-risk women of raising a child with fragile-X syndrome.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 15, doi. 10.1111/j.1399-0004.1989.tb03361.x

By:

Meryash, David L.

Publication type:

Article

Another case of Bloom's syndrome in Japan.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 77, doi. 10.1111/j.1399-0004.1989.tb03372.x

By:

Ishikiriyama, Satoshi

Publication type:

Article

Angiokeratoma corporis diffusum in G.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 59, doi. 10.1111/j.1399-0004.1989.tb03367.x

By:

Beratis, Nicholas G.;
Varvarigou-Frimas, Anastasia;
Beratis, Stavroula;
Sklower, Susan L.

Publication type:

Article

Albinism and skin cancer in Southern Africa.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 43, doi. 10.1111/j.1399-0004.1989.tb03365.x

By:

Kromberg, Jennifer G. R.;
Castle, David;
Zwane, Esther M.;
Jenkins, Trefor

Publication type:

Article

The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 25, doi. 10.1111/j.1399-0004.1989.tb03362.x

By:

Tuckerman, E.;
Webb, T.

Publication type:

Article

De novo Robertsonian D/D type translocations: the Leuven experience.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 65, doi. 10.1111/j.1399-0004.1989.tb03368.x

By:

Kleczkowska, A.;
Fryns, J. P.;
Standaert, L.;
Berghe, H.

Publication type:

Article

Holt-Oram syndrome associated with the hypoplastic left heart syndrome.

Published in:

Clinical Genetics, 1989, v. 36, n. 1, p. 69, doi. 10.1111/j.1399-0004.1989.tb03369.x

By:

Glauser, Tracy A.;
Zackai, Elaine;
Weinberg, Paul;
Clancy, Robert

Publication type:

Article