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Results 1 - 10 of 11 for carpenter
  1. Carpenter syndrome 
    Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  2. Alpha thalassemia X-linked intellectual disability syndrome 
    Alpha thalassemia X-linked intellectual disability syndrome is an inherited disorder that affects many parts of the body. This condition occurs almost exclusively ...
    https://medlineplus.gov/...x-linked-intellectual-disability-syndrome - Genetics
  3. Allan-Herndon-Dudley syndrome 
    ... article on PubMed Central Schwartz CE, May MM, Carpenter NJ, Rogers RC, Martin J, Bialer MG, Ward ...
    https://medlineplus.gov/.../condition/allan-herndon-dudley-syndrome - Genetics
  4. Central core disease 
    ... or Free article on PubMed Central Robinson R, Carpenter D, Shaw MA, Halsall J, Hopkins P. Mutations ...
    https://medlineplus.gov/genetics/condition/central-core-disease - Genetics
  5. Andermann syndrome 
    ... Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Hereditary motor and sensory neuropathy ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  6. Riboflavin transporter deficiency neuronopathy 
    ... Oppenheim M, Hargreaves I, Land JM, Wang MX, Carpenter K, Horvath R, Straub V, Lek M, Gold ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  7. Sotos syndrome 
    ... Singh MM, Gardner JE, Veerappan CS, Rice JC, Carpenter PB. Role for the nuclear receptor-binding SET ...
    https://medlineplus.gov/genetics/condition/sotos-syndrome - Genetics
  8. CLN11 disease 
    ... on PubMed Smith KR, Damiano J, Franceschetti S, Carpenter S, Canafoglia L, Morbin M, Rossi G, Pareyson ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
  9. Carney complex 
    ... article on PubMed Central Carney JA, Gordon H, Carpenter PC, Shenoy BV, Go VL. The complex of ...
    https://medlineplus.gov/genetics/condition/carney-complex - Genetics
  10. Idiopathic infantile hypercalcemia 
    ... INFANTILE, 1; HCINF1 HYPERCALCEMIA, INFANTILE, 2; HCINF2 PubMed Carpenter TO. CYP24A1 loss of function: Clinical phenotype of ...
    https://medlineplus.gov/.../idiopathic-infantile-hypercalcemia - Genetics
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