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
A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.
Liu M et al.
Journal of Human Genetics, 2006
A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family.
Fontaine K et al.
Genetic Counseling (geneva, Switzerland), 2005
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