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OMIM - Congenital disorder
OMIM - Growth hormone deficiency
OMIM - Intellectual disability
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X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity.
X-linked gene transcription patterns in female and male in vivo, in vitro and cloned porcine individ…
High nucleosome occupancy is encoded at X-linked gene promoters in C. elegans.
PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder.
Chromosomal redistribution of male-biased genes in mammalian evolution with two bursts of gene gain …
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Gene Transfer for X-Linked Severe Combined Immunodeficiency in Newly Diagnosed Infants
Study of RS1 Ocular Gene Transfer for X-linked Retinoschisis
Stem Cell Gene Therapy to Treat X-Linked Severe Combined Immunodeficiency (XSCID)
Gene Transfer Clinical Study in X-Linked Myotubular Myopathy
Gene Therapy for X Linked Severe Combined Immunodeficiency
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