Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 421, doi. 10.1111/j.1399-0004.1998.tb03757.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1998 AND VI 54 AND IP 5
Results: 15
1
2
Developmental delay, expressive aphasia, hypotonia and dysmorphism in two brothers: an X-linked mental retardation syndrome?
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 443, doi. 10.1111/j.1399-0004.1998.tb03762.x
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- Publication type:
- Article
3
HotSpots.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 380, doi. 10.1111/j.1399-0004.1998.tb03750.x
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- Publication type:
- Article
4
Charcot-Marie-Tooth phenotype produced by a duplicated PMP22 gene as part of a 17P trisomy-translocation to the X chromosome.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 413, doi. 10.1111/j.1399-0004.1998.tb03755.x
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- Publication type:
- Article
5
No association between the androgen receptor gene CAG repeat and impaired sperm production in Swedish men.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 435, doi. 10.1111/j.1399-0004.1998.tb03759.x
- Publication type:
- Article
6
Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephaly.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 406, doi. 10.1111/j.1399-0004.1998.tb03754.x
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- Publication type:
- Article
7
Announcements.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 446, doi. 10.1111/j.1399-0004.1998.tb03763.x
- Publication type:
- Article
8
Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 417, doi. 10.1111/j.1399-0004.1998.tb03756.x
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- Publication type:
- Article
9
Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 394, doi. 10.1111/j.1399-0004.1998.tb03752.x
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- Publication type:
- Article
10
Genetic testing and insurance in the United Kingdom.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 375, doi. 10.1111/j.1399-0004.1998.tb03749.x
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- Publication type:
- Article
11
Severe malformations in males from families with osteopathia striata with cranial sclerosis.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 400, doi. 10.1111/j.1399-0004.1998.tb03753.x
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- Publication type:
- Article
12
Two brothers with hypospadias, hypertelorism, upper lid coloboma and mixed type hearing loss: a new syndrome.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 440, doi. 10.1111/j.1399-0004.1998.tb03761.x
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- Publication type:
- Article
13
Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 426, doi. 10.1111/j.1399-0004.1998.tb03758.x
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- Publication type:
- Article
14
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L).
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 437, doi. 10.1111/j.1399-0004.1998.tb03760.x
- By:
- Publication type:
- Article
15
Genetic variants of the human obesity ( OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weight.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 5, p. 385, doi. 10.1111/j.1399-0004.1998.tb03751.x
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- Publication type:
- Article