Description of another case of 3q26.33-3q27.2 microdeletion supports a recognizable phenotype

Eur J Med Genet. 2013 Nov;56(11):624-5. doi: 10.1016/j.ejmg.2013.09.004. Epub 2013 Sep 18.

Authors

Yuri A Zarate¹, Carla Bell, Brad Schaefer

Affiliation

¹ Section of Genetics and Metabolism, Arkansas Children's Hospital, 1 Children's Way, Slot 512-22, Little Rock, AR 72202, USA. Electronic address: yazarate@uams.edu.

PMID: 24055528
DOI: 10.1016/j.ejmg.2013.09.004

No abstract available

Publication types

Case Reports
Letter
Comment

MeSH terms

Chromosomes, Human, Pair 3 / genetics*
Dentofacial Deformities / genetics*
Developmental Disabilities / genetics*
Female
Humans
Male
Muscle Hypotonia / genetics*
Sequence Deletion*