Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH.

Mencarelli, Maria Antonietta

Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH. [electronic resource] - American journal of medical genetics. Part A Apr 2007 - 858-65 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1552-4825

10.1002/ajmg.a.31602 doi


Abnormalities, Multiple--genetics
Chromosome Deletion
Chromosomes, Human, Pair 2
Craniofacial Abnormalities
Family Health
Humans
Infant, Newborn
Intellectual Disability
Male
Mental Disorders
Nucleic Acid Hybridization
Oligonucleotide Array Sequence Analysis
Sleep Wake Disorders