Associated Papers
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
Ma C et al.
Bmc Medical Genetics, 2019
Genetic abnormalities in fibrodysplasia ossificans progressiva.
Miao J et al.
Genes & Genetic Systems, 2012
Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients.
Lucotte G et al.
Genetic Counseling (geneva, Switzerland), 2009
Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva.
Sémonin O et al.
American Journal of Medical Genetics, 2001
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