Works matching IS 00099163 AND DT 1991 AND VI 39 AND IP 1

Results: 13

Tetrasomy 9p: an emerging syndrome.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 60, doi. 10.1111/j.1399-0004.1991.tb02986.x

By:

Jalal, S. M.;
Kukolich, Mary K.;
Garcia, Mary;
Benjamin, Toni R.;
Day, Donald W.

Publication type:

Article

Glyceryl ethers in peroxisomal disease.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 13, doi. 10.1111/j.1399-0004.1991.tb02980.x

By:

Poulos, A.;
Bankier, A.;
Beckman, K.;
Johnson, D.;
Robertson, E. F.;
Sharp, P.;
Sheffield, L.;
Singh, H.;
Usher, S.;
Wise, G.

Publication type:

Article

Dizygotic twins concordant for truncus arteriosus.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 75, doi. 10.1111/j.1399-0004.1991.tb02989.x

By:

Lang, Michael J.;
Aughton, David J.;
Riggs, Thomas W.;
Milad, Magdy P.;
Biesecker, Leslie G.

Publication type:

Article

Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 68, doi. 10.1111/j.1399-0004.1991.tb02988.x

By:

Murano, I.;
Ohashi, H.;
Tsukahara, M.;
Tonoki, H.;
Okino, F.;
Atsumi, M.;
Kajii, T.

Publication type:

Article

Anthropometric study with emphasis on hand and foot measurements in the Prader-Willi syndrome: sex, age and chromosome effects.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 39, doi. 10.1111/j.1399-0004.1991.tb02983.x

By:

Butler, Merlin G.;
Haynes, Judy L.;
Meaney, F. John

Publication type:

Article

A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 6, doi. 10.1111/j.1399-0004.1991.tb02979.x

By:

Skare, James C.;
Milunsky, Jeffrey M.;
Milunsky, Aubrey;
Skare, Ilze B.;
Cohen, Alan S.;
Skinner, Martha

Publication type:

Article

Coronary artery disease and apolipoprotein A-I/C-III gene polymorphism: a study of Saudi Arabians.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 1, doi. 10.1111/j.1399-0004.1991.tb02978.x

By:

Johansen, Klaus;
Dunn, Bruce;
Tan, Jenny C. Y.;
Kwaasi, Aaron A. A.;
Skotnicki, Antek;
Skotnickl, Mary

Publication type:

Article

Announcement.

Published in:: Clinical Genetics, 1991, v. 39, n. 1, p. 80, doi. 10.1111/j.1399-0004.1991.tb02990.x
Publication type:: Article

Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 33, doi. 10.1111/j.1399-0004.1991.tb02982.x

By:

Poulton, J.;
Deadman, M. E.;
Turnbull, D. M.;
Lake, B.;
Gardiner, R. M.

Publication type:

Article

Inv dup (8) (p21.1 → 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 55, doi. 10.1111/j.1399-0004.1991.tb02985.x

By:

Gorinati, Marino;
Caufin, Daniele;
Minelli, Antonella;
Memo, Luigi;
Gaspardo, Gianfranco;
Dodero, Andrea

Publication type:

Article

Genetic studies of human apolipoproteins. XVI. APOE polymorphism and cholesterol levels in the Mayans of the Yucatan Peninsula, Mexico.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 26, doi. 10.1111/j.1399-0004.1991.tb02981.x

By:

Kamboh, M. I.;
Weiss, K. M.;
Ferrell, R. E.

Publication type:

Article

Age of onset in vitiligo: relationship with HLA supratypes.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 48, doi. 10.1111/j.1399-0004.1991.tb02984.x

By:

Finco, O.;
Cuccia, M.;
Martinetti, M.;
Ruberto, G.;
Orecchia, G.;
Rabbiosi, G.

Publication type:

Article

Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardation.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 65, doi. 10.1111/j.1399-0004.1991.tb02987.x

By:

Lazarus, Arthur L.;
Moore, Kenneth E.;
Spinner, Nancy B.

Publication type:

Article