Pages that link to "Q56383962"

The following pages link to A paternal wash in Apert syndrome (Q56383962):

Displaying 7 items.

• Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D) (Q24517929) (← links)
• The high spontaneous mutation rate: Is it a health risk? (Q24603867) (← links)
• Paternal factors and schizophrenia risk: de novo mutations and imprinting (Q34356609) (← links)
• Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution (Q34387480) (← links)
• Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome (Q34447091) (← links)
• An aetiological classification of birth defects for epidemiological research (Q35446830) (← links)
• Molecular evolution—who is in the driver's seat? (Q50930753) (← links)