Pages that link to "Q41341329"

The following pages link to Dominance and homozygosity (Q41341329):

Displaying 14 items.

• A functionally dominant mitochondrial DNA mutation (Q33979047) (← links)
• Autosomal recessive diseases among Palestinian Arabs (Q34743125) (← links)
• Homozygosity of the autosomal dominant Alzheimer disease presenilin 1 E280A mutation (Q35106511) (← links)
• Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage (Q36017101) (← links)
• Consanguinity, endogamy, and genetic disorders in Tunisia. (Q36884581) (← links)
• Novel insights into the pathomechanisms of skeletal muscle channelopathies (Q37956141) (← links)
• A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23. (Q43145771) (← links)
• Homozygosity for a FBN1 missense mutation: clinical and molecular evidence for recessive Marfan syndrome (Q49051408) (← links)
• An homozygous mutation in KCNK3 is associated with an aggressive form of hereditary pulmonary arterial hypertension. (Q50224901) (← links)
• Type I collagen glomerulopathy: postnatal collagen deposition follows glomerular maturation (Q50702438) (← links)
• Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1. (Q52943915) (← links)
• Consanguinity and recurrence risk of stillbirth and infant death (Q56092575) (← links)
• Individual QTLs controlling quantitative variation in blood pressure inherited in a Mendelian mode (Q79374967) (← links)
• A Nonsense Mutation in COL4A4 Gene Causing Isolated Hematuria in Either Heterozygous or Homozygous State (Q91939040) (← links)