Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.

Authors :: Hernando C
Plaja A
Rigola MA
Pérez MM
Vendrell T
Egocue J
Fuster C
Source :: Journal of medical genetics [J Med Genet] 2002 May; Vol. 39 (5), pp. E24.
Publication Year :: 2002

Subjects :: Abnormalities, Multiple diagnosis
Humans
Infant, Newborn
Male
Nucleic Acid Hybridization
Phenotype
Abnormalities, Multiple genetics
Chromosome Deletion
Chromosomes, Human, Pair 16 ultrastructure

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