Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome. [electronic resource]
Producer: 20040728Description: 313-7 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- genetics
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- Craniofacial Abnormalities -- pathology
- DiGeorge Syndrome -- genetics
- Family Health
- Female
- Genotype
- Haplotypes
- Heart Defects, Congenital -- pathology
- Humans
- Male
- Microsatellite Repeats
- Pedigree
- Syndrome
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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