BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 4019538)

  • 21. Proximal symphalangism of fingers associated with fusion of os naviculare and talus and occurrence of two accessory bones in the feet (os paranaviculare and os tibiale externum) in an European--Indonesian--Chinese family.
    Wildervanck LS; Goedhard G; Meijer S
    Acta Genet Stat Med; 1967; 17(1):166-77. PubMed ID: 5633139
    [No Abstract]   [Full Text] [Related]  

  • 22. Tarsal-carpal coalition syndrome: importance of early diagnosis.
    Lau GTY; Athalye-Jape G; Amery N
    BMJ Case Rep; 2019 Jun; 12(6):. PubMed ID: 31175114
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary symphalangism with associated tarsal synostosis and hypophalangism.
    Castle JE; Bass S; Kanat IO
    J Am Podiatr Med Assoc; 1993 Jan; 83(1):1-9. PubMed ID: 8419625
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Natural Progression and Symptomatic Management of Tarsal-Carpal Coalition Syndrome: A Case Report.
    Berg AR; Pletcher BA; Edobor-Osula OF
    JBJS Case Connect; 2021 Oct; 11(4):. PubMed ID: 34714811
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar).
    Langer LO; Gorlin RJ; Donnai D; Hamel BC; Clericuzio C
    Am J Med Genet; 1994 May; 51(1):1-8. PubMed ID: 8030662
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiple synostoses syndrome: Clinical report and retrospective analysis.
    Pan Z; Lu W; Li X; Huang S; Dai P; Yuan Y
    Am J Med Genet A; 2020 Jun; 182(6):1438-1448. PubMed ID: 32259393
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.
    Ganaha A; Kaname T; Akazawa Y; Higa T; Shinjou A; Naritomi K; Suzuki M
    J Hum Genet; 2015 Jan; 60(1):27-34. PubMed ID: 25391606
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital malformation of the feet with low body height. A new syndrome, caused by an autosomal dominant gene.
    Gregersen HN; Petersen GB
    Clin Genet; 1977 Nov; 12(5):255-62. PubMed ID: 589846
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies.
    Coêlho KE; Ramos ES; Felix TM; Martelli L; de Pina-Neto JM; Niikawa N
    Am J Med Genet; 1998 Apr; 77(1):12-5. PubMed ID: 9557886
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.
    Takahashi T; Takahashi I; Komatsu M; Sawaishi Y; Higashi K; Nishimura G; Saito H; Takada G
    Clin Genet; 2001 Dec; 60(6):447-51. PubMed ID: 11846737
    [TBL] [Abstract][Full Text] [Related]  

  • 31.
    Clarke RA; Fang Z; Murrell D; Sheriff T; Eapen V
    Genes (Basel); 2021 Aug; 12(9):. PubMed ID: 34573339
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Symptomatic talonavicular coalition.
    Doyle SM; Kumar SJ
    J Pediatr Orthop; 1999; 19(4):508-10. PubMed ID: 10413002
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A new family with the hand-foot-genital syndrome--a wider spectrum of the hamd-foot-uterus syndrome.
    Poznanski AK; Kuhns LR; Lapides J; Stern AM
    Birth Defects Orig Artic Ser; 1975; 11(4):127-35. PubMed ID: 1156681
    [No Abstract]   [Full Text] [Related]  

  • 34. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
    Kantaputra PN; Gorlin RJ; Langer LO
    Am J Med Genet; 1992 Dec; 44(6):730-7. PubMed ID: 1481840
    [TBL] [Abstract][Full Text] [Related]  

  • 35. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Holt-Oram syndrome (analysis of six cases).
    Tunçbilek E; Ozme S; Besim A; Balci S
    Turk J Pediatr; 1980; 22(3-4):50-8. PubMed ID: 7256891
    [No Abstract]   [Full Text] [Related]  

  • 37. Fuhrmann syndrome associated with cortical dysplasia.
    Aynaci FM; Aynaci O; Ahmetoğlu A; Celep F
    Genet Couns; 2001; 12(1):49-54. PubMed ID: 11332978
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal dominant spondylocarpotarsal synostosis syndrome: phenotypic homogeneity and genetic heterogeneity.
    Isidor B; Cormier-Daire V; Le Merrer M; Lefrancois T; Hamel A; Le Caignec C; David A; Jacquemont S
    Am J Med Genet A; 2008 Jun; 146A(12):1593-7. PubMed ID: 18470895
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spondylocarpotarsal synostosis syndrome (with a posterior midline unsegmented bar).
    Al Kaissi A; Ghachem MB; Nassib N; Ben Chehida F; Kozlowski K
    Skeletal Radiol; 2005 Jun; 34(6):364-6. PubMed ID: 15891931
    [TBL] [Abstract][Full Text] [Related]  

  • 40. F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family.
    Camera G; Camera A; Pozzolo S; Costa M; Mantero R
    Am J Med Genet; 1995 Jul; 57(3):472-5. PubMed ID: 7677153
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.