Ramer JC, Ladda RL, Frankel CA, Beckford A
A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. [Case Reports, Journal Article, Review]
Am J Med Genet 1989 Mar; 32(3):359-63.
We report an infant with del(2)(q31q33). His phenotype is compared with those of the 7 children reported previously with the apparently identical deletion. Nine cases of deletions involving other segments of chromosome 2q are reviewed. Common manifestations of the 2 groups include small size at birth, growth and developmental retardation, cardiovascular malformation, microcephaly, and cleft palate.
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