Ryan A. Housam

Pediatrics
3322 US Highway 22
Branchburg, NJ 08876

Last Updated: 09/26/2026

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Found 1 publications

Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features.

Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features.

Journal: American journal of medical genetics. Part A
Published: August 16, 2012
Showing 1-1 of 1

Last Updated: 09/26/2026