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Publications by Augusta M A Lachmeijer
CRTAP Mutations in Lethal and Severe Osteogenesis Imperfecta: The Importance of Combining Biochemical and Molecular Genetic Analysis
European Journal of Human Genetics
Genetics
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Splints in Severe Osteogenesis Imperfecta.
BMJ
WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
American Journal of Human Genetics
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Osteogenesis Imperfecta - Clinical and Molecular Diversity
Osteogenesis Imperfecta
Osteogenesis Imperfecta
American Journal of Obstetrics and Gynecology
Gynecology
Obstetrics
The Role of Pamidronate in Pediatric Patients With Severe Osteogenesis Imperfecta
Journal of Pediatric Pharmacology and Therapeutics
Child Health
Pediatrics
Perinatology
Pharmacology
Corrigendum: Prolyl 3-Hydroxylase 1 Deficiency Causes a Recessive Metabolic Bone Disorder Resembling Lethal/Severe Osteogenesis Imperfecta
Nature Genetics
Genetics
Osteogenesis Imperfecta
Osteogenesis Imperfecta