These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 19693998)

  • 21. Novel human pathological mutations. Gene symbol: RHO. Disease: Retinitis pigmentosa.
    Yang J
    Hum Genet; 2009 Aug; 126(2):336. PubMed ID: 19694008
    [No Abstract]   [Full Text] [Related]  

  • 22. Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.
    Garcia-Planells J; Torres-Puente M; Vilchez JJ; Perez-Alonso M
    Hum Genet; 2009 Aug; 126(2):338. PubMed ID: 19694014
    [No Abstract]   [Full Text] [Related]  

  • 23. Novel human pathological mutations. Gene symbol: ECM1. Disease: Lipoid Proteinosis.
    Hameed A; Nasir M; Ajmal M; Latif L
    Hum Genet; 2009 Aug; 126(2):336. PubMed ID: 19694009
    [No Abstract]   [Full Text] [Related]  

  • 24. Novel human pathological mutations. Gene symbol: HBA2. Disease: Thalassemia alpha.
    Refaldi C; Fasulo MR; Cesaretti C; Cappellini MD
    Hum Genet; 2009 Aug; 126(2):342. PubMed ID: 19694027
    [No Abstract]   [Full Text] [Related]  

  • 25. Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency.
    Pretorius C; McMahon SK; Ungerer JP; Salmon N; Comwell L; Louise JA
    Hum Genet; 2009 Aug; 126(2):337. PubMed ID: 19694013
    [No Abstract]   [Full Text] [Related]  

  • 26. Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
    Di Pierro E; Brancaleoni V; Stanzial F; Benedicenti F; Castellan C; Cappellini MD
    Hum Genet; 2009 Aug; 126(2):339. PubMed ID: 19694018
    [No Abstract]   [Full Text] [Related]  

  • 27. Novel human pathological mutations. Gene symbol: PROC. Disease: Protein C deficiency.
    Pathare A; Al Zadjali S; Shah W
    Hum Genet; 2009 Aug; 126(2):336-7. PubMed ID: 19694010
    [No Abstract]   [Full Text] [Related]  

  • 28. Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
    Iascone M; Marchetti D; Lincesso AR; Iacovoni A; Ferrazzi P
    Hum Genet; 2009 Aug; 126(2):351. PubMed ID: 19694058
    [No Abstract]   [Full Text] [Related]  

  • 29. Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.
    Iascone MR; Marchetti D; Lincesso AR; Iacovoni A; Ferrazzi P
    Hum Genet; 2009 Aug; 126(2):351. PubMed ID: 19694057
    [No Abstract]   [Full Text] [Related]  

  • 30. Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophica.
    Cuadrado-Corrales N; Garcia M; Escamez MJ; Carrillo A; Trujillo-Tiebas MJ; Ayuso C; Del Rio M
    Hum Genet; 2009 Aug; 126(2):334. PubMed ID: 19694003
    [No Abstract]   [Full Text] [Related]  

  • 31. Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria.
    Chatzikyriakidou A; Kollios KD; Georgiou I
    Hum Genet; 2009 Aug; 126(2):335. PubMed ID: 19694006
    [No Abstract]   [Full Text] [Related]  

  • 32. Novel human pathological mutations. Gene symbol: APC. Disease: Adenomatous polyposis coli.
    Mavrogiannis LA; Chu CE; Charlton RS
    Hum Genet; 2009 Aug; 126(2):333-4. PubMed ID: 19694001
    [No Abstract]   [Full Text] [Related]  

  • 33. Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophica.
    Cuadrado-Corrales N; Garcia M; Escamez MJ; Carrillo A; Trujillo-Tiebas MJ; Ayuso C; Del Rio M
    Hum Genet; 2009 Aug; 126(2):335. PubMed ID: 19694005
    [No Abstract]   [Full Text] [Related]  

  • 34. Novel human pathological mutations. Gene symbol: COL7A1. Disease: Epidermolysis bullosa dystrophica.
    Garcia M; Escamez MJ; Cuadrado-Corrales N; Carrillo A; Trujillo-Tiebas MJ; Ayuso C; Del Rio M
    Hum Genet; 2009 Aug; 126(2):334-5. PubMed ID: 19694004
    [No Abstract]   [Full Text] [Related]  

  • 35. Molecular aspects of Rh antigens.
    Iwamoto S
    Leg Med (Tokyo); 2005 Jul; 7(4):270-3. PubMed ID: 15946885
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy.
    Provenzano G; Mannarino E; Annesi F; De Marco EV; Rocca FE; Greco V; Scornaienchi V; Tarantino P; Civitelli D; Quattrone A; Tortorella G; Annesi G
    Hum Genet; 2009 Aug; 126(2):337. PubMed ID: 19694011
    [No Abstract]   [Full Text] [Related]  

  • 37. Prevalence of RHD 1227A and hybrid Rhesus box in the general Chinese population.
    Yang YF; Wang YH; Chen JC; Eng HL; Lin TM
    Transl Res; 2007 Jan; 149(1):31-6. PubMed ID: 17196520
    [TBL] [Abstract][Full Text] [Related]  

  • 38. In-frame triplet deletions in RHD alter the D antigen phenotype.
    Flegel WA; Eicher NI; Doescher A; Hustinx H; Gowland P; Mansouri Taleghani B; Petershofen EK; Bauerfeind U; Ernst M; von Zabern I; Schrezenmeier H; Wagner FF
    Transfusion; 2006 Dec; 46(12):2156-61. PubMed ID: 17176329
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Comparison of Rhesus boxes in Hans and Uighurs].
    Lan JC; Zhou HY; Bai XH; Pang GZ; Wang XZ; Cai LJ; Cao Q; Zhang YZ; Xia R; Yang QK
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Oct; 22(5):580-2. PubMed ID: 16215956
    [TBL] [Abstract][Full Text] [Related]  

  • 40. DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
    Flegel WA; von Zabern I; Doescher A; Wagner FF; Vytisková J; Písacka M
    Transfusion; 2008 Jan; 48(1):25-33. PubMed ID: 17900276
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.