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At a Glance
Heterotopia, periventricular, autosomal recessive; ATR-X syndrome; Acquired hemoglobin H disease more...
ARFGEF2 (20q13.13); ASPM (1q31.3); ATR (3q23); ATRX (Xq21.1); CASC5 (15q15.1) more...
Conditions Help
Total conditions: 37
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
Technical Information
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Additional Information

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