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Whole mitochondrial genome analyses of Han population from Shandong of China using massively parallel sequencing. [PDF]
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Cytogenetic and Genome Research, 1962
Cytogenetic studies of 77 individuals, including 13 mongols, in six families are described. Chromosomal abnormalities which are segregating include a 13–15/21 type translocation (three families), a 21/22 translocation (one family), and a deletion of the short arm of chromosome no. 21 (one family).
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Cytogenetic studies of 77 individuals, including 13 mongols, in six families are described. Chromosomal abnormalities which are segregating include a 13–15/21 type translocation (three families), a 21/22 translocation (one family), and a deletion of the short arm of chromosome no. 21 (one family).
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The Irish Journal of Medical Science, 1960
A review of the possible pathogenesis in the mongoloid is presented. The problem of diagnosis in early infancy is emphasized and additional diagnostic criteria submitted, based onx-ray anomalies in the pelvis of the young mongoloid. Attention is drawn to the sociological and psychological problems associated with mongolism.
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A review of the possible pathogenesis in the mongoloid is presented. The problem of diagnosis in early infancy is emphasized and additional diagnostic criteria submitted, based onx-ray anomalies in the pelvis of the young mongoloid. Attention is drawn to the sociological and psychological problems associated with mongolism.
openaire +2 more sources