Pages that link to "Q52582798"
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The following pages link to A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q. (Q52582798):
Displaying 6 items.
- Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25 (Q24622683) (← links)
- Copy-number variations associated with autism spectrum disorder (Q37235652) (← links)
- Nine year old boy with chromosome 1q23.3-q25.1 deletion. (Q52859788) (← links)
- Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disability. (Q53089907) (← links)
- Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings. (Q53150475) (← links)
- Narrowing down the region responsible for 1q23.3q24.1 microdeletion by identifying the smallest deletion (Q90912888) (← links)