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Results 1 - 10 of 28 for turner syndrome
  1. Turner syndrome is a chromosomal condition that affects development in people who are assigned female at birth. Females typically have two X chromosomes, but ...
  2. ... cell is sufficient to cause the disorder. Familial Turner syndrome Female pseudo-Turner syndrome Male Turner syndrome Noonan's syndrome Noonan-Ehmke syndrome NS Pseudo- ...
  3. ... Hereditary osteo-onychodysplasia Osterreicher syndrome Pelvic horn syndrome Turner-Kieser syndrome Genetic Testing Registry: Nail-patella syndrome Nail-patella ...
  4. ... of these genetic conditions, such as Down syndrome, Turner syndrome, and 22q11.2 deletion syndrome, result from changes ...
  5. ... material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females. Am J Med Genet ...
  6. ... childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome. J Pediatr. 2005 Oct;147(4):499-507. ...
  7. ... 2-o. Citation on PubMed Cohen MM Jr, Turner JT, Biesecker LG. Proteus syndrome: misdiagnosis with PTEN mutations. Am J Med Genet ... on PubMed or Free article on PubMed Central Turner JT, Cohen MM Jr, ... syndrome literature: application of diagnostic criteria to published cases. ...
  8. ... Stanley C, Berry M, Irvine AD, Goudie D, Turner C, Brewer C, Smithson S. Cantu syndrome: report of nine new cases and expansion of ...
  9. ... Moreno-De-Luca D, Myers SM, Levy RV, Turner S, Ledbetter DH, Martin CL. 17q12 Recurrent Deletion Syndrome. 2016 Dec 8 [updated 2020 Oct 15]. In: ...
  10. ... for Rare Disorders (NORD) ClinicalTrials.gov MCCUNE-ALBRIGHT SYNDROME; MAS PubMed Boyce AM, Turner A, Watts L, Forestier-Zhang L, Underhill A, Pinedo-Villanueva R, Monsell F, Tessaris D, Burren C, Masi L, Hamdy N, Brandi ... an international multidisciplinary workshop to inform an international ...
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