A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family.

Fontaine, K; Sémonin, O; Legarde, J P; Lenoir, G; Lucotte, G

Fontaine, K; Sémonin, O; Legarde, J P; Lenoir, G; Lucotte, G.

Affiliation

Fontaine K; European Sequence Gene, Cybergène, Evry, France.

Genet Couns ; 16(2): 149-54, 2005.

Article in En | MEDLINE | ID: mdl-16080294

Subject(s)

DNA Mutational Analysis; Myositis Ossificans/genetics; Adenosine; Carrier Proteins; Chromosomes, Human, Pair 17; Genetic Carrier Screening; Guanine; Hallux Valgus/diagnosis; Hallux Valgus/genetics; Humans; Infant, Newborn; Male; Myositis Ossificans/diagnosis; Pedigree; Peptides/genetics; Sequence Analysis, DNA

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Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Myositis Ossificans Type of study: Diagnostic_studies Limits: Humans / Male / Newborn Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2005 Document type: Article Affiliation country: France Country of publication: Switzerland

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