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Adult-onset hereditary pulmonary alveolar proteinosis caused by a single-base deletion in CSF2RB,
Posted on by BMJ in Uncategorized
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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy,
Posted on by BMJ in Uncategorized
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Genetic architecture of open-angle glaucoma and related determinants,
Posted on by BMJ in Uncategorized
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GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms,
Posted on by BMJ in Uncategorized
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Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability,
Posted on by BMJ in Uncategorized
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Uptake of breast cancer prevention and screening trials,
Posted on by BMJ in Uncategorized
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Variants in CFTR untranslated regions are associated with congenital bilateral absence of the vas deferens,
Posted on by BMJ in Uncategorized
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Modeling the genetic risk prediction of type 1 diabetes,
Posted on by BMJ in Uncategorized
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Genetic issues in BCG Vaccination,
Posted on by BMJ in Uncategorized
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Welcome to JMG Contact,
Posted on by BMJ in Uncategorized
