Results 1 - 10 of 753 for Adams
  1. Adams-Oliver syndrome is a rare condition that is present at birth. The primary features are an ...
  2. ... metalloprotease domain with thrombospondin type I repeats 10 ADAM metallopeptidase with thrombospondin type 1 motif, 10 ADAM-TS10 ADAMTS-10 ATS10_HUMAN Tests of ADAMTS10 ...
  3. ... reprolysin type) with thrombospondin type 1 motif, 2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 ADAM-TS2 ATS2_HUMAN hPCPNI NPI PCINP PCPNI pNPI ...
  4. ... thrombotic thrombocytopenic purpura. More About This Health Condition ADAM metallopeptidase with thrombospondin type 1 motif, 13 ADAMTS- ...
  5. ... the NOTCH1 gene have been found to cause Adams-Oliver syndrome, a condition characterized by areas of ... Some of the NOTCH1 gene mutations involved in Adams-Oliver syndrome lead to production of an abnormally ...
  6. ... EOGT gene have been found in individuals with Adams-Oliver syndrome. This condition is characterized by areas ... or how it leads to the features of Adams-Oliver syndrome. More About This Health Condition AER61 ...
  7. ... nerve cells. Mutations in the DOCK6 gene cause Adams-Oliver syndrome, a condition characterized by areas of ... intellectual disability, are more common in DOCK6-related Adams-Oliver syndrome than in cases associated with other ...
  8. ... gene mutations have been found in people with Adams-Oliver syndrome, a condition characterized by areas of ... may underlie blood vessel abnormalities in people with Adams-Oliver syndrome; however, some people with DLL4-related ...
  9. ... 2002 Aug 29 [updated 2014 Jan 23]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean ... 2002 Aug 30 [updated 2020 Sep 24]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean ...
  10. ... Disorders (NORD) ClinicalTrials.gov MOWAT-WILSON SYNDROME PubMed Adam MP, Conta J, Bean LJH. Mowat-Wilson Syndrome. 2007 Mar 28 [updated 2019 Jul 25]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean ...
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