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