Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation

Two cases of primary ring chromosome 2 and one case of a ring secondary to a paternal 2/6 translocation are described and compared with a fourth case of ring 2 from the literature. The breakpoints in two cases are identical and the same as the breakpoint on chromosome 2 in the composite 2/6 ring. Th...

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Veröffentlicht in:	Human genetics 1979-04, Vol.48 (2), p.157-167
Hauptverfasser:	Maraschio, P, Danesino, C, Garau, A, Saputo, V, Vigi, V, Volpato, S
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - genetics Chromosome Aberrations Chromosome Mapping Chromosomes, Human, 1-3 Chromosomes, Human, 6-12 and X Endopeptidases - genetics Female Foot Deformities, Congenital Humans Infant Infant, Newborn Malate Dehydrogenase - genetics Male Translocation, Genetic
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