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Article

CALL gene is haploinsufficient in a 3p? syndrome patient

29 Oct 1999

Abstract excerpt

The 3p- syndrome results from deletion of a terminal segment of the short arm of one chromosome 3 (3p25-->pter), and is characterized by multiple congenital anomalies and mental retardation. Due to its variable expression, it is assumed this disorder is a contiguous gene syndrome with an undefined number of genes contributing to the phenotype. In an effort to discover genes contributing to mental defects in 3p-...

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Identifiers

PMID: 10508992
DOI: 10.1002/(sici)1096-8628(19991029)86:5<482::aid-ajmg15>3.0.co;2-l

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CALL gene is haploinsufficient in a 3p? syndrome patientPMID 10508992Read ↗

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