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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
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