Interstitial deletion of chromosome 13 and associated congenital anomalies
Copyright policy ) W W, Nichols; R C, Miller; E, Hoffman; D, Albert; R R, Weichselbaum; J, Nove; J B, Little;
Interstitial deletion of chromosome 13 and associated congenital anomalies
An interstitial deletion of chromosome 13 with breakpoints at 13q22 and 13q32 is presented. The clinical findings associated with this deletion are discussed in relation to the correlations of specific chromosomal bands with constellations of congenital defects as described by Niebuhr and Ottosen (1973), Niebuhr (1977). Lewandowski and Yunis (1975), and Noel et al. (1976).
- Massachusetts Eye and Ear Infirmary United States
- Harvard University United States
- Premier Clinical Research Institute United States
Adult, Chromosome Aberrations, Karyotyping, Humans, Abnormalities, Multiple, Chromosome Disorders, Female, Chromosome Deletion, Chromosomes, Human, 13-15, Chromosome Banding
Adult, Chromosome Aberrations, Karyotyping, Humans, Abnormalities, Multiple, Chromosome Disorders, Female, Chromosome Deletion, Chromosomes, Human, 13-15, Chromosome Banding
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These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 27
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Top 10%
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