Pages that link to "Q73356675"
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The following pages link to Perinatal hypophosphatasia: diagnosis and detection of heterozygote carriers within the family (Q73356675):
Displaying 7 items.
- Identification of expressed sequence tags preferentially expressed in human placentas by in silico subtraction (Q31142155) (← links)
- Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement (Q36938338) (← links)
- Neonatal lethal hypophosphatasia: A case report and review of literature (Q60310029) (← links)
- G317D mutation in the tissue-nonspecific alkaline phosphatase gene associated with childhood hypophosphatasia in a German family (Q73131971) (← links)
- Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers (Q83000694) (← links)
- Clinical Practice Guidelines for Hypophosphatasia (Q89584211) (← links)
- Association of ALPL variants with serum alkaline phosphatase and bone traits in the general Japanese population: The Nagahama Study (Q92132855) (← links)