A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype
Am J Med Genet A
.
2012 Mar;158A(3):680-4.
doi: 10.1002/ajmg.a.34433.
Epub 2012 Feb 2.
Authors
Christina Evers
1
,
Johannes W G Janssen
,
Anna Jauch
,
Michael Bonin
,
Ute Moog
Affiliation
1
Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.
[email protected]
PMID:
22302716
DOI:
10.1002/ajmg.a.34433
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Chromosome Banding
Chromosome Deletion*
Chromosomes, Human, Pair 11*
Humans
Jacobsen Distal 11q Deletion Syndrome / genetics*
Karyotyping
Male
Phenotype