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 18 for Feingold syndrome 1
  1. Feingold syndrome 
    ... Feingold syndrome National Organization for Rare Disorders (NORD) FEINGOLD SYNDROME 1; FGLDS1 FEINGOLD SYNDROME 2; FGLDS2 PubMed Celli J, ... Citation on PubMed Marcelis CLM, de Brouwer APM. Feingold Syndrome 1. 2009 Jun 30 [updated 2019 Apr 4]. In: ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  2. MYCN gene 
    ... Citation on PubMed Marcelis CLM, de Brouwer APM. Feingold Syndrome 1. 2009 Jun 30 [updated 2019 Apr 4]. In: ... Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models. Nat Commun. 2018 Apr 10;9(1):1352. doi: 10.1038/s41467-018-03788-7. ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  3. MIR17HG gene 
    ... Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models. Nat Commun. 2018 Apr 10;9(1):1352. doi: 10.1038/s41467-018-03788-7. ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  4. Facts about Down Syndrome (Centers for Disease Control and Prevention)  
    Down Syndrome/Start Here ... Down Syndrome ... Centers for Disease Control and Prevention ... Down syndrome is a condition in which a person has an extra chromosome. ...
    https://www.cdc.gov/ncbddd/birthdefects/DownSyndrome.html - External Health Links
  5. Weill-Marchesani syndrome 
    ... Megarbane A, Samples J, Gorlin RJ, Alswaid A, Feingold J, Le Merrer M, Munnich A, Cormier-Daire V. Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome. Am J Med Genet A. 2003 Dec 1;123A(2):204-7. doi: 10.1002/ajmg. ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  6. Hand-foot-genital syndrome 
    ... Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 ...
    https://medlineplus.gov/.../condition/hand-foot-genital-syndrome - Genetics
  7. HOXA13 gene 
    ... Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics
  8. Chromosome 13 
    ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  9. Meier-Gorlin syndrome 
    ... Rare Disorders (NORD) ClinicalTrials.gov ... J, Harley ME, Aftimos S, Al-Aama JY, Bober M, Brown PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers ...
    https://medlineplus.gov/genetics/condition/meier-gorlin-syndrome - Genetics
  10. ORC1 gene 
    ... HSORC1 ORC1_HUMAN ORC1L origin recognition complex, subunit 1 origin recognition complex, subunit 1 homolog PARC1 replication control protein 1 Tests of ...
    https://medlineplus.gov/genetics/gene/orc1 - Genetics
previous · 1 · 2 · next