Proximal 15q variant with normal phenotype in three unrelated individuals.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 311, doi. 10.1111/j.1399-0004.1987.tb02814.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1987 AND VI 31 AND IP 5
Results: 15
1
2
Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 315, doi. 10.1111/j.1399-0004.1987.tb02815.x
- By:
- Publication type:
- Article
3
Effect of vitamin E and ticlopidine on platelet aggregation in Fabry's disease.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 349, doi. 10.1111/j.1399-0004.1987.tb02820.x
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- Publication type:
- Article
4
How do carriers of hemophilia experience prenatal diagnosis by fetal blood s ampling?
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 297, doi. 10.1111/j.1399-0004.1987.tb02811.x
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- Publication type:
- Article
5
Letters to the Editors: Reply to a response by Sherman & Iselius to comments on the segregation of balanced pericentric inversions.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 355, doi. 10.1111/j.1399-0004.1987.tb02821.x
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- Publication type:
- Article
6
The Angelman (Happy Puppet) syndrome: is it autosomal recessive?
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 323, doi. 10.1111/j.1399-0004.1987.tb02816.x
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- Publication type:
- Article
7
Announcement.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 358, doi. 10.1111/j.1399-0004.1987.tb02823.x
- Publication type:
- Article
8
Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects?
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 279, doi. 10.1111/j.1399-0004.1987.tb02809.x
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- Publication type:
- Article
9
Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 331, doi. 10.1111/j.1399-0004.1987.tb02817.x
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- Publication type:
- Article
10
Congenital cutis laxa.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 357, doi. 10.1111/j.1399-0004.1987.tb02822.x
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- Publication type:
- Article
11
Trichodysplasia-xeroderma: an autosomal dominant condition.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 337, doi. 10.1111/j.1399-0004.1987.tb02818.x
- By:
- Publication type:
- Article
12
Fragile sites are unrelated to reciprocal translocation breakpoints.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 308, doi. 10.1111/j.1399-0004.1987.tb02813.x
- By:
- Publication type:
- Article
13
Syndrome of microcephaly, deafness/ malformed ears, mental retardation and peculiar facies in a mother and son.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 303, doi. 10.1111/j.1399-0004.1987.tb02812.x
- By:
- Publication type:
- Article
14
Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature review.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 343, doi. 10.1111/j.1399-0004.1987.tb02819.x
- By:
- Publication type:
- Article
15
Female carriers of Duchenne muscular dystrophy: a dilemma.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 5, p. 288, doi. 10.1111/j.1399-0004.1987.tb02810.x
- By:
- Publication type:
- Article