Results 91 -
100
of
1,114
for
RA
- ... In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ... Taylor CT, Maisenbacher MK, Versluys B, Newbury-Ecob RA, Ozsahin H, Damin MK, Bowen VM, McCurdy KR, ...
- ... In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ... In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ...
- ... JBA, Malovannaya A, Martin JF, Rosenblatt DS, Poche RA. Mutations in Hcfc1 and Ronin result in an ... H, Forgetta V, Dobson CM, Leclerc D, Gravel RA, Shoubridge EA, Coulton JW, Lepage P, Rommens JM, ...
- ... Disorders (NORD) ClinicalTrials.gov TRIMETHYLAMINURIA; TMAU PubMed Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA. Diagnosis and management of trimethylaminuria (FMO3 deficiency) in ...
- ... MJ, Roeffen M, Hamel BC, Weaving L, Ouvrier RA, Donald JA, Wevers RA, Christodoulou J, van Bokhoven H. Arts syndrome is ... In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ...
- ... America (DebRA) Fine JD, Bruckner-Tuderman L, Eady RA, Bauer EA, Bauer JW, Has C, Heagerty A, ... In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ...
- ... C, Didona B, Zambruno G, Patrizi A, Eady RA, McGrath JA. Recurrent mutations in kindlin-1, a ... F, Zaghloul AB, Hamada T, Mallipeddi R, Eady RA, McLean WH, McGrath JA, Epstein EH. Loss of ...
- ... X; PDHX NCBI Gene ClinVar Brown RM, Head RA, Brown GK. Pyruvate dehydrogenase E3 binding protein deficiency. ... Jan 22. Citation on PubMed Brown RM, Head RA, Morris AA, Raiman JA, Walter JH, Whitehouse WP, ...
- ... This Health Condition MedlinePlus Genetics provides information about Rheumatoid arthritis More About This Health Condition MedlinePlus Genetics provides ...
- ... U, Matthijs G, Hennet T, Jaeken J, Wevers RA. Clinical and biochemical characteristics of congenital disorder of ... PubMed Imbach T, Burda P, Kuhnert P, Wevers RA, Aebi M, Berger EG, Hennet T. A mutation ...