Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome. [electronic resource]
Producer: 19690108Description: 609-14 p. digitalISSN:- 0002-922X
- Adult
- Blood Group Antigens
- Child
- Chromosome Aberrations
- Chromosomes, Human, 13-15
- Chromosomes, Human, 21-22 and Y
- Chromosomes, Human, 6-12 and X
- Dermatoglyphics
- Down Syndrome -- genetics
- Duodenal Obstruction -- complications
- Female
- Heart Defects, Congenital -- complications
- Humans
- Hyperbilirubinemia -- complications
- Infant, Newborn
- Karyotyping
- Male
- Mitosis
- Mosaicism
- Pedigree
- Sex Chromosomes
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Publication Type: Journal Article
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