Pages that link to "Biology:Compound heterozygosity"
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The following pages link to Biology:Compound heterozygosity:
Displayed 25 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Biology:Mutation (← links)
- Biology:Phosphoglycerate dehydrogenase (← links)
- Biology:SLC22A5 (← links)
- Biology:IFT140 (← links)
- Medicine:Leigh syndrome (← links)
- Medicine:Autosomal recessive polycystic kidney disease (← links)
- Medicine:Pantothenate kinase-associated neurodegeneration (← links)
- Medicine:Phenylketonuria (← links)
- Medicine:Cerebroretinal microangiopathy with calcifications and cysts (← links)
- Medicine:Neu–Laxova syndrome (← links)
- Medicine:Neu-Laxova syndrome (← links)
- Medicine:Oculocutaneous albinism type I (← links)
- Medicine:Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (← links)
- Medicine:D-glycerate dehydrogenase deficiency (← links)
- Medicine:Tay–Sachs disease (← links)
- Medicine:Jalili syndrome (← links)
- Medicine:Beta thalassemia (← links)
- Medicine:Yunis–Varon syndrome (← links)
- Medicine:Dopamine transporter deficiency syndrome (← links)
- Medicine:Upshaw–Schulman syndrome (← links)
- Medicine:Hypodysfibrinogenemia (← links)
- Medicine:Hypotrichosis with juvenile macular dystrophy (← links)
- Medicine:Kenny-Caffey syndrome (← links)
- Medicine:Hypophosphatasia (← links)
- Medicine:Lipoprotein lipase deficiency (← links)
