Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 30 for complete analysis
  1. Aniridia 
    ... van Heyningen V, Beal SJ, Crolla JA. Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia. Am J Med Genet A. 2008 Mar 1;146A(5):558-69. doi: 10.1002/ajmg.a.32209. Citation on PubMed
    https://medlineplus.gov/genetics/condition/aniridia - Genetics
  2. Recurrent hydatidiform mole 
    ... RA. Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype ... and epigenetic analysis of recurrent hydatidiform mole. Hum Mutat. 2009 May; ...
    https://medlineplus.gov/.../condition/recurrent-hydatidiform-mole - Genetics
  3. Androgenetic alopecia 
    ... of prostate cancer: a systematic review and meta-analysis. J Am Acad Dermatol. 2013 Jun;68(6):937-43. doi: 10.1016/j.jaad.2012.11.034. Epub 2013 Feb 8. Citation on PubMed Cousen P, Messenger A. Female pattern hair loss in complete androgen insensitivity syndrome. Br J Dermatol. 2010 May; ...
    https://medlineplus.gov/genetics/condition/androgenetic-alopecia - Genetics
  4. Obstructive sleep apnea 
    ... H, Yin S. A systematic review and meta-analysis of the association between serotonergic gene polymorphisms and obstructive sleep apnea syndrome. PLoS One. 2014 Jan 27;9(1):e86460. doi: 10.1371/journal.pone.0086460. eCollection 2014. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/obstructive-sleep-apnea - Genetics
  5. Primary spontaneous pneumothorax 
    ... space) that can result in the partial or complete collapse of a lung. This type of pneumothorax ... CG, Lin J, Qiao D, Yi L. Mutation analysis of the FLCN gene in Chinese patients with ...
    https://medlineplus.gov/.../primary-spontaneous-pneumothorax - Genetics
  6. Oculocutaneous albinism 
    ... on PubMed Central Kamaraj B, Purohit R. Mutational analysis of oculocutaneous albinism: a compact review. Biomed Res ...
    https://medlineplus.gov/genetics/condition/oculocutaneous-albinism - Genetics
  7. Inherited thyroxine-binding globulin deficiency 
    ... forms of inherited thyroxine-binding globulin deficiency: the complete form (TBG-CD), which results in a total ... binding globulin deficiency to avoid unnecessary treatments. The complete form of inherited thyroxine-binding globulin deficiency, TBG- ...
    https://medlineplus.gov/...ted-thyroxine-binding-globulin-deficiency - Genetics
  8. Blepharophimosis, ptosis, and epicanthus inversus syndrome 
    ... to difficulty conceiving a child (subfertility) or a complete inability to conceive (infertility). The prevalence of BPES ... cannot open fully. Mutations that lead to a complete loss of FOXL2 protein function often cause BPES ...
    https://medlineplus.gov/...s-ptosis-and-epicanthus-inversus-syndrome - Genetics
  9. Trisomy 13 
    ... chromosome 13 to their children. Bartholin-Patau syndrome Complete trisomy 13 syndrome Patau syndrome Patau's syndrome Trisomy 13 syndrome Genetic Testing Registry: Complete trisomy 13 syndrome Trisomy 13 National Organization for ...
    https://medlineplus.gov/genetics/condition/trisomy-13 - Genetics
  10. Osteoarthritis 
    ... osteoarthritis, leading to cartilage damage and, over time, complete breakdown. Without the protection of the cartilage, bone ... Reynard LN, Loughlin J. The genetics and functional analysis of primary osteoarthritis susceptibility. Expert Rev Mol Med. ...
    https://medlineplus.gov/genetics/condition/osteoarthritis - Genetics
previous · 1 · 2 · 3 · next