Works matching IS 00099163 AND DT 1979 AND VI 15 AND IP 2
Results: 19
Familial holoprosencephaly.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 203, doi. 10.1111/j.1399-0004.1979.tb01763.x
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- Article
Announcements.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 207, doi. 10.1111/j.1399-0004.1979.tb01767.x
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- Article
A simple method to detect linkage for rare recessive diseases: An application to juvenile diabetes.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 126, doi. 10.1111/j.1399-0004.1979.tb01751.x
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- Article
Electronic data processing in the Danish Cytogenetic Central Register and EDP problems of registers in general.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 137, doi. 10.1111/j.1399-0004.1979.tb01752.x
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- Article
Ichthyosis vulgaris.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 206, doi. 10.1111/j.1399-0004.1979.tb01766.x
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- Article
Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 183, doi. 10.1111/j.1399-0004.1979.tb01759.x
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- Article
Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 176, doi. 10.1111/j.1399-0004.1979.tb01758.x
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- Article
Autosomal recessive onychotrichodysplasia, chronic neutropenia and mild mental retardation.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 147, doi. 10.1111/j.1399-0004.1979.tb01753.x
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- Article
Uttrastructure of skin biopsy specimens in lysosomal storage diseases: Common sources of error in diagnosis.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 118, doi. 10.1111/j.1399-0004.1979.tb01750.x
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- Article
Orientation of major histocompatibility (MHC) genes relative to the centromere of human chromosome 6.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 198, doi. 10.1111/j.1399-0004.1979.tb01762.x
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- Article
Variable expression in a dominantly inherited skeletal dysplasia with similarities to brachydactyly E and spondyloepiphyseal- spondyloperipheral dysplasia.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 160, doi. 10.1111/j.1399-0004.1979.tb01755.x
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- Article
'Adult' form of polycystic kidney disease in neonates.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 205, doi. 10.1111/j.1399-0004.1979.tb01765.x
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- Article
Counseling for dominant traits: a correction for the ascertainment bias due to referral for analysis.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 171, doi. 10.1111/j.1399-0004.1979.tb01757.x
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- Article
Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 113, doi. 10.1111/j.1399-0004.1979.tb01749.x
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- Article
Monoamine oxidase and catechol-o-m ethyl transferase activity in cultured fibroblasts from patients with maple syrup urine disease, Lesch-Nyhan syndrome and healthy controls.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 153, doi. 10.1111/j.1399-0004.1979.tb01754.x
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- Article
C-band polymorphism in human chromosome no. 6.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 193, doi. 10.1111/j.1399-0004.1979.tb01761.x
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- Article
Reply to Escobar and Cantu.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 204, doi. 10.1111/j.1399-0004.1979.tb01764.x
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- Article
Trisomy 20q due to maternal t(16;20) translocation First case.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 2, p. 167, doi. 10.1111/j.1399-0004.1979.tb01756.x
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- Article
Melkersson- Rosenthal's syndrome in four generations.
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- Clinical Genetics, 1979, v. 15, n. 2, p. 189, doi. 10.1111/j.1399-0004.1979.tb01760.x
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- Article