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 51 - 60 of 81 for Miller syndrome
  1. ATM gene 
    ... 70.002. Citation on PubMed Kurz EU, Lees-Miller SP. DNA damage-induced activation ... and related syndromes. Radiother Oncol. 2007 Jun;83(3):231-7. ...
    https://medlineplus.gov/genetics/gene/atm - Genetics
  2. Chromosome 2 
    ... Eddy SR, Marra MA, Ovcharenko I, Furey TS, Miller W, Eichler EE, Bork P, Suyama M, ... syndrome: an update of the clinical spectrum including overweight, ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
  3. IFT140 gene 
    ... Mainzer-Saldino syndrome. Disorders such as Mainzer-Saldino syndrome that are caused by problems with cilia and involve bone abnormalities ... Behal RH, Miller MS, Qin H, Lucker BF, Jones A, Cole ...
    https://medlineplus.gov/genetics/gene/ift140 - Genetics
  4. SUCLA2 gene 
    ... AW, Scaglia F. SUCLA2-Related Mitochondrial DNA Depletion Syndrome, ... Elpeleg O, Miller C, Hershkovitz E, Bitner-Glindzicz M, Bondi-Rubinstein ...
    https://medlineplus.gov/genetics/gene/sucla2 - Genetics
  5. ANTXR2 gene 
    ... available. Citation on PubMed Liu S, Crown D, Miller-Randolph S, ... LT. Hyaline Fibromatosis Syndrome. 2008 Feb 27 [updated 2023 May 11]. In: ...
    https://medlineplus.gov/genetics/gene/antxr2 - Genetics
  6. 16p11.2 deletion syndrome 
    ... Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, ... A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  7. SCN4A gene 
    ... on PubMed Miller TM, Dias da Silva MR, Miller HA, Kwiecinski H, ... Engel AG. Myasthenic syndrome caused by mutation of the SCN4A sodium channel. ...
    https://medlineplus.gov/genetics/gene/scn4a - Genetics
  8. COG5-congenital disorder of glycosylation 
    ... and symptoms of the condition. Carbohydrate deficient glycoprotein ... Epub 2011 Sep 22. Citation on PubMed or Free article on PubMed Central Miller VJ, Sharma P, Kudlyk TA, Frost L, Rofe ...
    https://medlineplus.gov/...cog5-congenital-disorder-of-glycosylation - Genetics
  9. Y chromosome 
    ... 0b013e31811ec1b4. Citation on PubMed Russo P, Siani A, ... new look at XXYY syndrome: medical and psychological features. Am J Med Genet ...
    https://medlineplus.gov/genetics/chromosome/y - Genetics
  10. SMCHD1 gene 
    ... novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and ... Bamshad MJ, Tapscott SJ, Miller DG, van der Maarel SM. Digenic inheritance of ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · next