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Xq28
Summary
General Info
Curated Studies
Most Correlated Studies
HCFC1 regulatory mutation in nonsyndromic intellectual disability (NS-ID) patients
Leydig tumor MLTC-1 cells transfected with MAMLD-1 siRNA
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Literature
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Possible incomplete penetrance of Xq28 int22h-1/int22h-2 duplication.
Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete p…
Exploring inheritance, and clinical penetrance of distal Xq28 duplication syndrome: insights from 47…
Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion.
The int22h1/int22h2-Mediated Xq28 Duplication Syndrome: An Intersection between Neurodevelopment, Im…
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Pilot Study of the Effects of the Desipramine on the Neurovegetative Parameters of the Child With Re…
Study of Genotype and Phenotype Expression in Congenital Nephrogenic Diabetes Insipidus
Effects of Creatine Supplementation in Rett Syndrome
Independent Studies of Dextromethorphan and of Donepezil Hydrochloride for Rett Syndrome
Molecular Associations With Reproductive Failure
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