'Pure' partial trisomy 11q (11q23.1→11qter): expanding the phenotype

Clin Dysmorphol. 2011 Oct;20(4):225-228. doi: 10.1097/MCD.0b013e328349bcf8.

Authors

Avishag Zimberg-Bossira¹, Tatiana Smolkin, Anna Gildish, Nivin Moustafa-Hawash, Shraga Blazer, Ruth Gershoni-Baruch, Imad R Makhoul

Affiliation

¹ Departments of Medical Genetics Neonatology, Meyer Children's Hospital, Rambam Health Care Campus, and the Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa, Israel.

PMID: 21900761
DOI: 10.1097/MCD.0b013e328349bcf8

No abstract available

Publication types

Case Reports

MeSH terms

Abnormal Karyotype
Adult
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 21
Humans
Infant
Infant, Newborn
Male
Phenotype*
Translocation, Genetic
Trisomy / diagnosis*

Supplementary concepts

Chromosome 11, partial trisomy 11q