Pages that link to "Q71308118"
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The following pages link to Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN (Q71308118):
Displaying 6 items.
- Epigenomic strategies at the interface of genetic and environmental risk factors for autism (Q37638802) (← links)
- Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3. (Q42129638) (← links)
- Angelman syndrome in an inbred family. (Q52009028) (← links)
- Prenatal diagnosis of a fetus with a homologous Robertsonian translocation of chromosomes 15 (Q73691843) (← links)
- Methylation analysis at three different loci within the imprinted region of chromosome 15q11–13 (Q73691863) (← links)
- Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15 (Q74460767) (← links)