Works matching IS 00099163 AND DT 1984 AND VI 26 AND IP 2
Results: 14
Male to male transmission of the G syndrome.
- Published in:
- Clinical Genetics, 1984, v. 26, n. 2, p. 164, doi. 10.1111/j.1399-0004.1984.tb00808.x
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- Article
Mentally retarded siblings with congenital heart defect, peculiar facies and cryptorchidism in the male: possible McDonough syndrome with coincidental (X; 20) translocation.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 117, doi. 10.1111/j.1399-0004.1984.tb00800.x
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- Article
Combined sialidase (neuraminidase) and β-galactosidase deficiency. Clinical, morphological and enzymological observations in a patient.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 139, doi. 10.1111/j.1399-0004.1984.tb00804.x
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- Article
Selection against genetic defects in semen donors.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 87, doi. 10.1111/j.1399-0004.1984.tb00798.x
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- Article
A young girl with ring(18) mosaicism: cytogenetic studies and PEP A mapping.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 156, doi. 10.1111/j.1399-0004.1984.tb00806.x
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- Article
Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I disease.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 109, doi. 10.1111/j.1399-0004.1984.tb00799.x
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- Article
Mandibuloacral dysplasia: a rare progeroid syndrome Two brothers confirm autosomal recessive inheritance.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 133, doi. 10.1111/j.1399-0004.1984.tb00803.x
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- Article
Chromosome studies on normal males in 16 families with the marker X chromosome.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 166, doi. 10.1111/j.1399-0004.1984.tb00810.x
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- Article
Manifestations and natural history of idiopathic hemihypertrophy: a review of eleven cases.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 81, doi. 10.1111/j.1399-0004.1984.tb00797.x
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- Article
Mosaic tetrasomy 21 in a male child.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 150, doi. 10.1111/j.1399-0004.1984.tb00805.x
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- Article
Prader-Willi syndrome in Black females.
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- Clinical Genetics, 1984, v. 26, n. 2, p. 161, doi. 10.1111/j.1399-0004.1984.tb00807.x
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- Article
Fragile 22q13 segregating in a family.
- Published in:
- Clinical Genetics, 1984, v. 26, n. 2, p. 125, doi. 10.1111/j.1399-0004.1984.tb00801.x
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- Article
Monosomy X associated with fra(17p12) and 22p-.
- Published in:
- Clinical Genetics, 1984, v. 26, n. 2, p. 165, doi. 10.1111/j.1399-0004.1984.tb00809.x
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- Article
Genetics of site specific colon cancer: a family study.
- Published in:
- Clinical Genetics, 1984, v. 26, n. 2, p. 129, doi. 10.1111/j.1399-0004.1984.tb00802.x
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- Article