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See Latest ArticlesALX4 dysfunction disrupts craniofacial and epidermal development
Human Molecular Genetics, 11/05/09
Kayserili H et al. – The data indicate that ALX4 plays a critical role both in craniofacial development as in skin and hair follicle development in human.
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Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
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Familial atypical cold urticaria: Description of a new hereditary disease
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Accumulation of gene polymorphisms related to plaque disruption and thrombosis is associated with cerebral infarction in subjects with type 2 diabetes
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Accumulation of gene polymorphisms related to plaque disruption and thrombosis is associated with cerebral infarction in subjects with type 2 diabetes
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Accumulation of gene polymorphisms related to plaque disruption and thrombosis is associated with cerebral infarction in subjects with type 2 diabetes
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Accumulation of gene polymorphisms related to plaque disruption and thrombosis is associated with cerebral infarction in subjects with type 2 diabetes
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