Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 151, doi. 10.1111/j.1399-0004.1979.tb00984.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1979 AND VI 16 AND IP 3
Results: 12
1
2
A chromosome survey of a hospital for the mentally subnormal.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 191, doi. 10.1111/j.1399-0004.1979.tb00990.x
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- Publication type:
- Article
3
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 137, doi. 10.1111/j.1399-0004.1979.tb00982.x
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- Publication type:
- Article
4
Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 183, doi. 10.1111/j.1399-0004.1979.tb00989.x
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- Publication type:
- Article
5
Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 147, doi. 10.1111/j.1399-0004.1979.tb00983.x
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- Publication type:
- Article
6
Oculodento-osseous dysplasia: heterogeneity or variable expression?
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 169, doi. 10.1111/j.1399-0004.1979.tb00987.x
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- Publication type:
- Article
7
Five familial cases with a trisomy 16p syndrome due to translocation.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 205, doi. 10.1111/j.1399-0004.1979.tb00991.x
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- Publication type:
- Article
8
The Japanese Society of Human Genetics.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 215, doi. 10.1111/j.1399-0004.1979.tb00992.x
- Publication type:
- Article
9
Features of trisomy 18 and 18p-syndromes in an infant with 46, XY, i(18q).
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 163, doi. 10.1111/j.1399-0004.1979.tb00986.x
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- Publication type:
- Article
10
International Symposium.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 215, doi. 10.1111/j.1399-0004.1979.tb00993.x
- Publication type:
- Article
11
Translocation 46XY, t (17;18) (q25;q21) in a mentally retarded boy with progressive eye abnormalities.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 156, doi. 10.1111/j.1399-0004.1979.tb00985.x
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- Publication type:
- Article
12
Two abnormal clones in the bone marrow cells of a patient with paroxysmal nocturnal hemoglobinuria.
- Published in:
- Clinical Genetics, 1979, v. 16, n. 3, p. 178, doi. 10.1111/j.1399-0004.1979.tb00988.x
- By:
- Publication type:
- Article