Mikara Amazon Music Stream millions of songs. In the two families, MED12 missense mutations c. HisAsn] in MED12 was detected. Get to Know Us. English Choose a language for shopping.
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Mikara Amazon Music Stream millions of songs. In the two families, MED12 missense mutations c. HisAsn] in MED12 was detected. Get to Know Us. English Choose a language for shopping. Find all citations in this journal default.
SerPro] segregating with the phenotype were identified. Amazon Rapids Fun stories for kids on the go. AmazonGlobal Ship Orders Internationally.
Abstract Ohdo syndrome comprises a heterogeneous group of disorders characterized by intellectual disability ID and typical facial features, including blepharophimosis. Please try your request again later.
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We performed exome sequencing in two families, each with two affected males with Ohdo syndrome MKB type. Gene Ontology GO Terms.
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