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Results 1 - 10 of 150 for Young syndrome
  1. ... variant Ohdo syndrome, SBBYS variant Say-Barber-Biesecker-Young-Simpson syndrome Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome SBBYS variant of Ohdo syndrome SBBYSS Young-Simpson syndrome Genetic Testing Registry: Blepharophimosis - intellectual disability syndrome, SBBYS ...
  2. ... article on PubMed Central Sarfati J, Dode C, Young J. Kallmann syndrome caused by mutations in the PROK2 and PROKR2 ...
  3. ... gov COFFIN-LOWRY SYNDROME; CLS PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002 ...
  4. ... do not survive past infancy, others live into young adulthood. Wiedemann-Rautenstrauch syndrome is a rare disorder. Its prevalence is unknown. ...
  5. ... Lannigan E. Neurobehavioral disorders in children, adolescents, and young adults with Down syndrome. Am J Med Genet C Semin Med Genet. ...
  6. ... to sit or walk without assistance. Babies and young children with FOXG1 syndrome often have feeding problems, sleep disturbances, seizures, irritability, ...
  7. ... phobias are common among people with this disorder.Young children with Williams syndrome have distinctive facial features including a broad forehead, ...
  8. ... 2003.06.001. Citation on PubMed Hanauer A, Young ID. Coffin-Lowry syndrome: clinical and molecular features. J Med Genet. 2002 ...
  9. ... Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and ...
  10. ... Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP. Kallmann syndrome: mutations in the genes encoding prokineticin-2 and ...
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