2q31.1 microdeletion syndrome: case report and literature review.

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2q31.1 microdeletion syndrome: case report and literature review.

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2q31.1 microdeletion syndrome: case report and literature review.

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2q31.1 microdeletion syndrome: case report and literature review.

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2q31.1 microdeletion syndrome: case report and literature review.

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P1476

2q31.1 microdeletion syndrome: case report and literature review.

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P2093

Arun Kashyap

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Chantal Bruno

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Melissa February

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Rajeev Mehta

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Surasak Puvabanditsin

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Tazeem Shaik

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P2860

Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster

Limb malformations and the human HOX genes

Synpolydactyly in mice with a targeted deficiency in the HoxD complex

Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).

Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review.

A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly.

Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.

Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.

Two cases with interstitial deletions of chromosome 2 and sex reversal in one.

Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation

P304

357-360

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P31

scholarly article

case report

P356

10.1002/CCR3.260

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P433

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P478

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P577

2015-03-29T00:00:00Z

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P5875

274321963

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P698

26185628

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P932

4498842

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