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Results 1 - 4 of 4 for Klippel Feil syndrome
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  1. Klippel-Feil syndrome 
    Klippel-Feil syndrome is a bone disorder characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae). The vertebral ...
    https://medlineplus.gov/genetics/condition/klippel-feil-syndrome - Genetics
  2. GDF6 gene 
    ... the GDF6 gene have been found to cause Klippel-Feil syndrome, a condition characterized by the abnormal joining (fusion) ... the body. Most GDF6 gene mutations that cause Klippel-Feil syndrome replace single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/gdf6 - Genetics
  3. GDF3 gene 
    ... the GDF3 gene have been found to cause Klippel-Feil syndrome, a condition characterized by the abnormal joining (fusion) ... of the body. GDF3 gene mutations that cause Klippel-Feil syndrome replace single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/gdf3 - Genetics
  4. MEOX1 gene 
    ... the MEOX1 gene have been found to cause Klippel-Feil syndrome. This condition is characterized by the abnormal joining ( ... HZ. Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype. BMC Genet. 2013 Sep 28;14:95. ...
    https://medlineplus.gov/genetics/gene/meox1 - Genetics