ZFHX4

Publications

Palomares M et al. Characterization of a 8q21.11 Microdeletion Syndrome Associated With Intellectual Disability and a Recognizable Phenotype. Am J Hum Genet. 2011;89(2):295-301.  PMID:21802062.

Hofmann K et al. 7 Mb De Novo Deletion Within 8q21 in a Patient With Distal Arthrogryposis Type 2B (DA2B). Eur J Med Genet. 2011;54(5):e495-500.  PMID:21722758.

Happ H et al. 8q21.11 Microdeletion in Two Patients With Syndromic Peters Anomaly. Am J Med Genet A. 2016;170(9):2471-2475.  PMID:27378168.

Vulto-van Silfhout AT et al. Clinical Significance of De Novo and Inherited Copy-Number Variation. Hum Mutat. 2013;34(12):1679-87.  PMID:24038936.

InĂ©s Quintela et al. Clinical Characterization of a Male Patient With the Recently Described 8q21.11 Microdeletion Syndrome. Am J Med Genet A. 2015;167(6):1369-73.  PMID:25898976.