Refinement of the 8q22.1 microdeletion critical region associated with Nablus mask-like facial syndrome

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2014-01, Vol.164A (1), p.259-263
Hauptverfasser:	Overhoff, Justin, Rabideau, Marina M., Bird, Lynne M., Schweitzer, Daniela N., Haynes, Karla, Schultz, Roger A., Shaffer, Lisa G., Rosenfeld, Jill A., Ellison, Jay W.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - diagnosis Abnormalities, Multiple - genetics Blepharophimosis - diagnosis Blepharophimosis - genetics Brain - pathology Child Chromosome Deletion Chromosomes, Human, Pair 8 Craniofacial Abnormalities - diagnosis Craniofacial Abnormalities - genetics Facies Genetic Association Studies Humans Infant Magnetic Resonance Imaging Male Phenotype
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