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 *

90 related articles for article (PubMed ID: 21479481)

  • 21. What syndrome is this? Beare-Stevenson cutis gyrata syndrome.
    Izakovic J; Leitner S; Schachner LA
    Pediatr Dermatol; 2003; 20(4):358-60. PubMed ID: 12869163
    [No Abstract]   [Full Text] [Related]  

  • 22. Mutational analysis of ras gene family in lung cancer in Thai.
    Petmitr S; Wongsommart D; Chaksangchaichot P; Pakeetoot T; Sutinont P; Sirivaidyapong P; Karalak A
    Oncol Rep; 2003; 10(5):1497-501. PubMed ID: 12883730
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Perioperative care of a patient with Beare-Stevenson syndrome.
    Upmeyer S; Bothwell M; Tobias JD
    Paediatr Anaesth; 2005 Dec; 15(12):1131-6. PubMed ID: 16324039
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations.
    Theiler M; Weibel L; Christen-Zaech S; Carmignac V; Sorlin A; Neuhaus K; Chevarin M; Thauvin-Robinet C; Philippe C; Faivre L; Vabres P; Kuentz P
    J Eur Acad Dermatol Venereol; 2021 Oct; 35(10):2085-2090. PubMed ID: 33930231
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Beare-Stevenson Syndrome With Blepharoptosis as a Complication of Front-Orbital Advancement and Remodeling.
    Platt A; Budden C; Badilla J; Pollock N; Louie G; Mehta V
    J Craniofac Surg; 2020 Sep; 31(6):1780-1781. PubMed ID: 32604297
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Congenital craniofacial dysostosis and cutis gyratum: the Beare-Stevenson syndrome.
    Bratanic B; Praprotnik M; Novosel-Sever M
    Eur J Pediatr; 1994 Mar; 153(3):184-6. PubMed ID: 8181503
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Beare-Stevenson cutis gyrata syndrome with Chiari malformation.
    Wang TJ; Hung KS; Chen PK; Chuang WL; Shih TY; Lai BJ; Hsiao M
    Acta Neurochir (Wien); 2002 Jul; 144(7):743-5. PubMed ID: 12181710
    [No Abstract]   [Full Text] [Related]  

  • 28. Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
    Chen CP; Lin SP; Su YN; Chien SC; Tsai FJ; Wang W
    Genet Couns; 2008; 19(2):165-72. PubMed ID: 18618990
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Association of gene polymorphisms with myocardial infarction in individuals with or without conventional coronary risk factors.
    Nishihama K; Yamada Y; Matsuo H; Segawa T; Watanabe S; Kato K; Yajima K; Hibino T; Yokoi K; Ichihara S; Metoki N; Yoshida H; Satoh K; Nozawa Y
    Int J Mol Med; 2007 Jan; 19(1):129-41. PubMed ID: 17143557
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Somatic mitochondrial mutations in melanoma resection specimens.
    Deichmann M; Kahle B; Benner A; Thome M; Helmke B; Näher H
    Int J Oncol; 2004 Jan; 24(1):137-41. PubMed ID: 14654950
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Strong association between lung cancer and the AXIN2 polymorphism.
    Gunes EG; Pinarbasi E; Pinarbasi H; Silig Y
    Mol Med Rep; 2009; 2(6):1029-35. PubMed ID: 21475939
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.
    Heller A; Fricke HJ; Starke H; Loncarevic IF; Claussen U; Liehr T
    Oncol Rep; 2004 Jan; 11(1):89-92. PubMed ID: 14654908
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation analysis of K-ras and beta-catenin genes related to O6-methylguanin-DNA methyltransferase and mismatch repair protein status in human gallbladder carcinoma.
    Kohya N; Kitajima Y; Kitahara K; Miyazaki K
    Int J Mol Med; 2003 Jan; 11(1):65-9. PubMed ID: 12469220
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel insertion in the FGFR2 gene in a patient with Crouzon phenotype and sacrococcygeal tail.
    Lapunzina P; Fernández A; Sánchez Romero JM; Delicado A; Sáenz de Pipaon M; López Pajares I; Molano J
    Birth Defects Res A Clin Mol Teratol; 2005 Jan; 73(1):61-4. PubMed ID: 15602758
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin.
    Wang PP; Lin M; Wu JR; Wang XY; Yang LY
    Mol Med Rep; 2010; 3(3):459-61. PubMed ID: 21472262
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Discrepancies between in silico and in vitro data in the functional analysis of a breast cancer-associated polymorphism in the XRCC6/Ku70 gene.
    Marras E; Willems P; Vandersickel V; Ceriani I; Thierens H; Vral A; Perletti G
    Mol Med Rep; 2008; 1(6):805-12. PubMed ID: 21479489
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Unusual form of Noonan syndrome: neonatal multi-organ involvement with chylothorax and nevoid Cutis verticis gyrata].
    Masson P; Fayon M; Lamireau T; Llanas B; Lacombe D; Taïeb A; Demarquez JL
    Pediatrie; 1993; 48(1):59-62. PubMed ID: 8392694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Multidisciplinary treatment for severe syndromic craniosynostosis].
    Uyama A; Kawamura A; Yamamoto K; Nagashima T; Nishimoto S; Oyama T; Nishijima E; Satoh S; Nakao H; Nomura K; Otsu M; Sakamoto K
    No Shinkei Geka; 2009 Jan; 37(1):25-34. PubMed ID: 19175030
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease.
    Marque M; Gardie B; Bressac de Paillerets B; Rustin P; Guillot B; Richard S; Bessis D
    Br J Dermatol; 2010 Dec; 163(6):1337-9. PubMed ID: 20560959
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cutis verticis gyrata: three cases with different aetiologies that demonstrate the classification system.
    Larsen F; Birchall N
    Australas J Dermatol; 2007 May; 48(2):91-4. PubMed ID: 17535195
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.