Short stature due to 15q26 microdeletion involving IGF1R: report of an additional case and review of the literature
Am J Med Genet A
.
2011 Dec;155A(12):3139-43.
doi: 10.1002/ajmg.a.34310.
Epub 2011 Nov 7.
Authors
Laura I Rudaks
1
,
Jillian K Nicholl
,
Drago Bratkovic
,
Christopher P Barnett
Affiliation
1
SA Clinical Genetics Service, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
PMID:
22065603
DOI:
10.1002/ajmg.a.34310
No abstract available
Publication types
Case Reports
Review
MeSH terms
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 15*
Dwarfism / diagnosis*
Dwarfism / genetics*
Facies
Female
Humans
Phenotype
Receptor, IGF Type 1 / genetics*
Substances
Receptor, IGF Type 1