A partial trisomy 1q patient with a deletion 1q22 and an insertion 1(q42q44) into 1q22

Am J Med Genet A. 2009 Feb;149A(2):290-3. doi: 10.1002/ajmg.a.32623.

Authors

Doriana Misceo¹, Mariano Rocchi, Carl Birger van der Hagen, Eirik Frengen

Affiliation

¹ Department of Medical Genetics, Ullevål University Hospital and Faculty of Medicine, University of Oslo, Oslo, Norway.

PMID: 19161140
DOI: 10.1002/ajmg.a.32623

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't
Review

MeSH terms

Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Cytogenetic Analysis
Face / abnormalities
Growth Disorders / genetics
Humans
Karyotyping
Male
Middle Aged
Sequence Deletion
Trisomy*