Works matching IS 00099163 AND DT 1988 AND VI 34 AND IP 4

Results: 12

Coffin-Lowry syndrome: a multicenter study.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 230, doi. 10.1111/j.1399-0004.1988.tb02870.x

By:

Gilgenkrantz, S.;
Mujica, P.;
Gruet, P.;
Tridon, P.;
Schweitzer, F.;
Nivelon-Chevallier, A.;
Nivelon, J. L.;
Couillault, G.;
David, A.;
Verloes, A.;
Lambotte, C.;
Piussan, Ch.;
Mathieu, M.

Publication type:

Article

Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 252, doi. 10.1111/j.1399-0004.1988.tb02872.x

By:

Wallis, C. E.

Publication type:

Article

PRUFILE: a clinical and laboratory database for the genetics centre.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 209, doi. 10.1111/j.1399-0004.1988.tb02867.x

By:

Mutton, D. E.;
Chown, K.;
Thomson, L.;
Berry, A. C.;
Botcherby, P. K.;
Bobrow, M.

Publication type:

Article

Terminal deletion of the short arm of chromosome 5.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 219, doi. 10.1111/j.1399-0004.1988.tb02868.x

By:

Baccichetti, C.;
Lenzini, E.;
Artifoni, L.;
Caufin, D.;
Marangoni, P.

Publication type:

Article

Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 272, doi. 10.1111/j.1399-0004.1988.tb02875.x

By:

Eiberg, Hans;
Marner, Else;
Rosenberg, Thomas;
Mohr, Jan

Publication type:

Article

Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 265, doi. 10.1111/j.1399-0004.1988.tb02874.x

By:

Anvret, Maria;
Gillberg, Christopher;
Wahlström, Jan;
Albertsson-Wikland, Kerstin;
Davies, Kay

Publication type:

Article

A photometer used for diagnosing a small-sized 4p deletion in Wolf syndrome.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 276, doi. 10.1111/j.1399-0004.1988.tb02876.x

By:

Léonard, C.;
Huret, J. L.

Publication type:

Article

Association of apolipoprotein ɛ4 allele with hypertriglyceridemia in obesity.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 258, doi. 10.1111/j.1399-0004.1988.tb02873.x

By:

Fumeron, F.;
Rigaud, D.;
Bertiere, M. C.;
Bardon, S.;
Dely, C.;
Apfelbaum, M.

Publication type:

Article

Announcements.

Published in:: Clinical Genetics, 1988, v. 34, n. 4, p. 282, doi. 10.1111/j.1399-0004.1988.tb02878.x
Publication type:: Article

Trisomy (1q) (q42→qter): confirmation of a syndrome.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 224, doi. 10.1111/j.1399-0004.1988.tb02869.x

By:

Chia, N. L.;
Bousfield, L. R.;
Poon, C. C. S.;
Trudinger, B. J.

Publication type:

Article

Apolipoprotein E alleles and hyperlipoproteinemia in Japan.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 246, doi. 10.1111/j.1399-0004.1988.tb02871.x

By:

Eto, M.;
Watanabe, K.;
Ishii, K.

Publication type:

Article

Mental retardation with pterygia, shortness and distinct facial appearance. Confirmation of a new MCA/MR syndrome.

Published in:

Clinical Genetics, 1988, v. 34, n. 4, p. 279, doi. 10.1111/j.1399-0004.1988.tb02877.x

By:

Schrander-Stumpel, C.;
Haspeslagh, M.;
Fryns, J. P.

Publication type:

Article