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Patient Individual

Gender	M
Type of diagnosis	Molecular
Diagnosis	8p23.1 MICRODELETION SYNDROME
MIM Number
Clinical phenotype	Affected
Molecular analysis	Not available

Patient samples ▼

ID	Sample type	Extraction Year
106605	Blood	2012	View
106606	EBV-Lymphoblast cell line	2013	View
106607	DNA	2016	View