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Article

4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate

2 Jul 2009

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Share to Congenital Ear and Nasal Anomalies
Share to Genomic variations and chromosomal abnormalities
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19576302
DOI: 10.1016/j.ejmg.2009.06.003

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Related research

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Research trail→

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4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palatePMID 19576302Read ↗

A novel 5q11.2 microdeletion in a child with mild developmental delay and dysmorphic features.Semantic proximity Read ↗

A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis.Semantic proximity Read ↗

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Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech.Semantic proximity Read ↗

Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion Syndrome.Semantic proximity Read ↗

The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomaliesSemantic proximity Read ↗

8p21 microdeletion in a patient with intellectual disability and behavioral abnormalities.Semantic proximity Read ↗

Molecular cytogenetic characterization of 2p23.2p23.3 deletion in a child with developmental delay, hypotonia and cryptorchism.Semantic proximity Read ↗

Clinical and molecular characterization of a patient with a 2q31.2‐32.3 deletion identified by array‐CGHSemantic proximity Read ↗

De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl With Developmental Delay, Speech Delay, Congenital Cleft Palate, and Bilateral Hearing Impairment.Semantic proximity Read ↗

Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.Semantic proximity Read ↗

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