Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q
Am J Med Genet A
.
2009 Feb;149A(2):277-9.
doi: 10.1002/ajmg.a.32617.
Authors
Hasibe Artac
1
,
Ismail Reisli
,
Mahmut Selman Yildirim
,
Gulseren Bagci
,
Guven Luleci
,
Orhan Hosgor
,
Sevim Karaaslan
Affiliation
1
Department of Pediatrics, Division of Immunology and Allergy, Selcuk University Meram Medical Faculty, Konya, Turkey.
[email protected]
PMID:
19161136
DOI:
10.1002/ajmg.a.32617
No abstract available
Publication types
Case Reports
MeSH terms
Agammaglobulinemia / genetics*
Aneuploidy*
Chromosomes, Human, Pair 21*
Chromosomes, Human, Pair 7*
Face / abnormalities
Humans
Infant
Male
Phenotype
Scoliosis