Works matching IS 00099163 AND DT 1985 AND VI 28 AND IP 2
Results: 20
The Eighth Annual New York March of Dimes Symposium on Genetics for the Practicing Physician.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 183, doi. 10.1111/j.1399-0004.1985.tb00384.x
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- Article
Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 136, doi. 10.1111/j.1399-0004.1985.tb00373.x
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- Article
The cerebro-costo-mandibular syndrome: third report of familial occurrence.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 118, doi. 10.1111/j.1399-0004.1985.tb00370.x
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- Article
Frequency of fragile X chromosome in normal females.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 97, doi. 10.1111/j.1399-0004.1985.tb00366.x
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- Article
Heterogeneity of Kallmann's syndrome.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 106, doi. 10.1111/j.1399-0004.1985.tb00368.x
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- Article
Cornelia de Lange syndrome in a mother and daughter.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 157, doi. 10.1111/j.1399-0004.1985.tb00376.x
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- Article
Imaging techniques in muscular dystrophies.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 179, doi. 10.1111/j.1399-0004.1985.tb00382.x
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- Article
EEC syndrome without ectrodactyly? Report of 8 cases.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 130, doi. 10.1111/j.1399-0004.1985.tb00372.x
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- Article
Partial trisomy 12q: clinical and cytogenetic observations.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 112, doi. 10.1111/j.1399-0004.1985.tb00369.x
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- Article
Heritable fragility at 11q13 and 12q13.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 145, doi. 10.1111/j.1399-0004.1985.tb00374.x
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- Article
46, X, i(Xq) karyotype in a patient with hypoplastic left heart.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 178, doi. 10.1111/j.1399-0004.1985.tb00381.x
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- Article
13th Annual Meeting of the European Working Group for Cystic Fibrosis.
- Published in:
- Clinical Genetics, 1985, v. 28, n. 2, p. 183, doi. 10.1111/j.1399-0004.1985.tb00385.x
- Publication type:
- Article
Age of onset in siblings of persons with juvenile Huntinqton disease.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 100, doi. 10.1111/j.1399-0004.1985.tb00367.x
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- Article
Prenatal testing and twinning.
- Published in:
- Clinical Genetics, 1985, v. 28, n. 2, p. 180, doi. 10.1111/j.1399-0004.1985.tb00383.x
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- Article
Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritance.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 151, doi. 10.1111/j.1399-0004.1985.tb00375.x
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- Article
Partial trisomy 5q and partial monosomy 5q within the same family.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 122, doi. 10.1111/j.1399-0004.1985.tb00371.x
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- Article
An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short arm.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 162, doi. 10.1111/j.1399-0004.1985.tb00377.x
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- Article
A new banding pattern of human chromosomes by in situ nick translation using ECO RI and biotin-dUTP.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 173, doi. 10.1111/j.1399-0004.1985.tb00379.x
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- Article
A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 166, doi. 10.1111/j.1399-0004.1985.tb00378.x
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- Article
About diploid-tetraploid mosaicism.
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- Clinical Genetics, 1985, v. 28, n. 2, p. 177, doi. 10.1111/j.1399-0004.1985.tb00380.x
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- Article