A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference14 articles.
1. Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46, XX, del(2) (q31q33)
2. Interstitial deletion 2q31→q33
3. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation
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2. Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay;Cytogenetic and Genome Research;2015
3. The role of SATB2 in skeletogenesis and human disease;Cytokine & Growth Factor Reviews;2014-02
4. A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report;Molecular Cytogenetics;2012-01-03
5. Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation;American Journal of Medical Genetics Part A;2011-05-12
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