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Results 1 - 10 of 20 for Fraser syndrome 1
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  1. FRAS1 gene 
    ... is unknown. extracellular matrix protein FRAS1 FLJ14927 FLJ22031 Fraser syndrome 1 KIAA1500 Tests of FRAS1 PubMed FRASER EXTRACELLULAR MATRIX COMPLEX SUBUNIT 1; FRAS1 CONGENITAL ANOMALIES ...
    https://medlineplus.gov/genetics/gene/fras1 - Genetics
  2. Fraser syndrome 
    ... Schwickerath syndrome Ullrich-Feichtiger syndrome Genetic Testing Registry: Fraser syndrome 1 Fraser syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/fraser-syndrome - Genetics
  3. FREM2 gene 
    ... Scambler PJ. Molecular study of 33 families with Fraser syndrome new data and mutation review. Am J Med Genet A. 2008 Sep 1;146A(17):2252-7. doi: 10.1002/ajmg. ...
    https://medlineplus.gov/genetics/gene/frem2 - Genetics
  4. Branchiootorenal/branchiootic syndrome 
    ... Branchiootorenal dysplasia Branchiootorenal spectrum disorders Branchiootorenal syndrome Melnick-Fraser syndrome ... Branchiootorenal syndrome 1 BOR syndrome ...
    https://medlineplus.gov/.../branchiootorenal-branchiootic-syndrome - Genetics
  5. GRIP1 gene 
    ... leads to kidney abnormalities and other problems in Fraser syndrome. More About This Health Condition ... PubMed GLUTAMATE RECEPTOR-INTERACTING ...
    https://medlineplus.gov/genetics/gene/grip1 - Genetics
  6. Axenfeld-Rieger syndrome 
    ... Semina EV. Current molecular understanding of Axenfeld-Rieger syndrome. Expert Rev Mol Med. 2005 Nov 8;7(25):1-17. doi: 10.1017/S1462399405010082. Citation on PubMed Idrees F, Vaideanu D, Fraser SG, Sowden JC, Khaw PT. A review of ...
    https://medlineplus.gov/genetics/condition/axenfeld-rieger-syndrome - Genetics
  7. Congenital anomalies of kidney and urinary tract 
    ... deletion syndrome, renal cysts and diabetes (RCAD) syndrome, Fraser syndrome, ... CAKUT is estimated to occur in 1 in 100 to 500 newborns. These abnormalities are ...
    https://medlineplus.gov/...tal-anomalies-of-kidney-and-urinary-tract - Genetics
  8. Clouston syndrome 
    ... ddh191. Epub 2004 Jun 22. Citation on PubMed Fraser FC, Der ... Med Genet 2001 Sep 1;102(4):394. Citation on PubMed Fujimoto A, ...
    https://medlineplus.gov/genetics/condition/clouston-syndrome - Genetics
  9. CYP11B2 gene 
    ... 2008 May 29. Citation on PubMed Connell JM, Fraser R, MacKenzie ... Fardella C. Genetics of hypertensive syndrome. Horm Res. 2009;71(5):253-9. doi: ...
    https://medlineplus.gov/genetics/gene/cyp11b2 - Genetics
  10. 1q21.1 microdeletion 
    ... 1q21.1 deletion syndrome Chromosome 1q21.1 deletion syndrome, 1.35-Mb Genetic Testing Registry: Chromosome 1q21.1 ... Disorders (NORD) ClinicalTrials.gov CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB PubMed Brunetti-Pierri N, Berg JS, ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
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