A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndrome.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 74, doi. 10.1111/j.1399-0004.1990.tb03550.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1990 AND VI 38 AND IP 1
Results: 12
1
2
Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 38, doi. 10.1111/j.1399-0004.1990.tb03545.x
- By:
- Publication type:
- Article
3
Families with X-linked liver glycogenosis due to phosphorylase kinase deficiency.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 80, doi. 10.1111/j.1399-0004.1990.tb03552.x
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- Publication type:
- Article
4
Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritance.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 51, doi. 10.1111/j.1399-0004.1990.tb03547.x
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- Publication type:
- Article
5
Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 1, doi. 10.1111/j.1399-0004.1990.tb03541.x
- By:
- Publication type:
- Article
6
Time trends (1980-1987) of ten selected informative morphogenetic variants in a newborn population.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 33, doi. 10.1111/j.1399-0004.1990.tb03544.x
- By:
- Publication type:
- Article
7
Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease?
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 44, doi. 10.1111/j.1399-0004.1990.tb03546.x
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- Publication type:
- Article
8
Pseudoinflammatory fundus dystrophy: a follow-up study.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 21, doi. 10.1111/j.1399-0004.1990.tb03543.x
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- Publication type:
- Article
9
Analysis of mosaic states in amniotic fluid using the in-situ colony technique.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 14, doi. 10.1111/j.1399-0004.1990.tb03542.x
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- Publication type:
- Article
10
Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome).
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 69, doi. 10.1111/j.1399-0004.1990.tb03549.x
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- Publication type:
- Article
11
Autosomal dominant familial spastic paraplegia: report of a large New England family.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 57, doi. 10.1111/j.1399-0004.1990.tb03548.x
- By:
- Publication type:
- Article
12
Trisomy of chromosome 20/isochrome 12p.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 1, p. 79, doi. 10.1111/j.1399-0004.1990.tb03551.x
- By:
- Publication type:
- Article