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 *

112 related articles for article (PubMed ID: 28762477)

  • 41. A novel
    Zhou S; Wang F; Dou Y; Zhou J; Hao G; Xu C; Wang QK; Wang H; Wang P
    Clin Case Rep; 2018 Aug; 6(8):1612-1617. PubMed ID: 30147916
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations.
    Frédéric MY; Monino C; Marschall C; Hamroun D; Faivre L; Jondeau G; Klein HG; Neumann L; Gautier E; Binquet C; Maslen C; Godfrey M; Gupta P; Milewicz D; Boileau C; Claustres M; Béroud C; Collod-Béroud G
    Hum Mutat; 2009 Feb; 30(2):181-90. PubMed ID: 18767143
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Congenital contractural arachnodactyly.
    Forbes D; Hagan R
    Med J Aust; 1983 Feb; 1(3):128. PubMed ID: 6571539
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Beals-Hecht syndrome (congenital contractural arachnodactyly) with additional craniospinal abnormality: a case report.
    Meena JP; Gupta A; Mishra D; Juneja M
    J Pediatr Orthop B; 2015 May; 24(3):226-9. PubMed ID: 25493702
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Arachnodactyly represented in art.
    Pyeritz RE
    Am J Med Genet C Semin Med Genet; 2021 Jun; 187(2):163-167. PubMed ID: 34021688
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the
    Yagi H; Takiguchi H; Takeda N; Inuzuka R; Taniguchi Y; Porto KJ; Ishiura H; Mitsui J; Morita H; Komuro I
    Clin Case Rep; 2022 Feb; 10(2):e05335. PubMed ID: 35154713
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Prenatal diagnosis in congenital contractural arachnodactyly.
    Belleh S; Spooner L; Allanson J; Godfrey M
    Genet Test; 1997-1998; 1(4):293-6. PubMed ID: 10464661
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Congenital contractural arachnodactyly.
    Kontras SB
    Birth Defects Orig Artic Ser; 1975; 11(6):63-7. PubMed ID: 1201352
    [No Abstract]   [Full Text] [Related]  

  • 49. Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.
    Tsipouras P; Del Mastro R; Sarfarazi M; Lee B; Vitale E; Child AH; Godfrey M; Devereux RB; Hewett D; Steinmann B
    N Engl J Med; 1992 Apr; 326(14):905-9. PubMed ID: 1542340
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Congenital contractural arachnodactyly (CCA syndrome)--an autosomal dominant hereditary connective tissue disease].
    Meinecke P; Schaefer E; Passarge E
    Klin Padiatr; 1983; 195(1):64-70. PubMed ID: 6834743
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Congenital contractural arachnodactyly in a black family.
    Steg NL
    Birth Defects Orig Artic Ser; 1975; 11(6):57-62. PubMed ID: 1201351
    [No Abstract]   [Full Text] [Related]  

  • 52. [Clinical diagnosis and surgical treatment of congenital contractural arachnodactyly: analysis of 6 cases].
    Wang XS; Zhang JG; Qiu GX; Weng XS; Gao ZX; Lu WC; Zhao LJ
    Zhonghua Yi Xue Za Zhi; 2008 Mar; 88(9):615-8. PubMed ID: 18646717
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Congenital contractural arachnodactyly (Beals-Hecht syndrome). Report of a familial case].
    Capdevila Sánchez J; Luaces Cubells C; Campistol Plana J; Alfonso Moncalvo H; Martín Pueyo G
    An Esp Pediatr; 1991 Nov; 35(5):353-5. PubMed ID: 1785753
    [No Abstract]   [Full Text] [Related]  

  • 54. Beals-Hecht syndrome.
    Jones JL; Lane JE; Logan JJ; Vanegas ME
    South Med J; 2002 Jul; 95(7):753-5. PubMed ID: 12144083
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A syndrome resembling congenital contractural arachnodactyly.
    Passarge E
    Birth Defects Orig Artic Ser; 1975; 11(6):53-6. PubMed ID: 1201350
    [No Abstract]   [Full Text] [Related]  

  • 56. Orofacial manifestations of congenital fibrillin deficiency: pathogenesis and clinical diagnostics.
    De Coster PJ; Martens LC; De Paepe A
    Pediatr Dent; 2004; 26(6):535-7. PubMed ID: 15646918
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Congenital contractural arachnodactyly (Beals-Hecht syndrome) associated with Brown's syndrome].
    Fehlow P
    Klin Monbl Augenheilkd; 2005 May; 222(5):440-3. PubMed ID: 15912465
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The metacarpophalangeal profile in a family with congenital contractural arachnodactyly.
    Guala A; Danesino C; Milewicz DM; Putnam EA; Franceschini P
    Genet Couns; 2000; 11(1):57-8. PubMed ID: 10756430
    [No Abstract]   [Full Text] [Related]  

  • 59. "New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896.
    Hecht F; Beals RK
    Pediatrics; 1972 Apr; 49(4):574-9. PubMed ID: 4552107
    [No Abstract]   [Full Text] [Related]  

  • 60. [The Beals-Hecht syndrome (congenital contractural arachnodactyly) revealed in a neonate].
    Philip N; Garcia-Meric P; Wernert F
    Pediatrie; 1988; 43(7):609-12. PubMed ID: 3200664
    [TBL] [Abstract][Full Text] [Related]  

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