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 *

79 related articles for article (PubMed ID: 8721058)

  • 21. Achondroplastic dog breeds have no mutations in the transmembrane domain of the FGFR-3 gene.
    Martínez S; Valdés J; Alonso RA
    Can J Vet Res; 2000 Oct; 64(4):243-5. PubMed ID: 11041504
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia.
    Orhant L; Anselem O; Fradin M; Becker PH; Beugnet C; Deburgrave N; Tafuri G; Letourneur F; Goffinet F; Allach El Khattabi L; Leturcq F; Bienvenu T; Tsatsaris V; Nectoux J
    Prenat Diagn; 2016 May; 36(5):397-406. PubMed ID: 26850935
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
    Gürgey A; Beksaç S; Mesci L; Cakar N; Karakaş U; Kutlar A; Altay C
    Turk J Pediatr; 1993; 35(3):159-62. PubMed ID: 7909397
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of cystic fibrosis in a Turkish family.
    Yilmaz E; Ozgüç M; Coşkun T; Beksaç S; Cakar N; Ayter S; Ozalp I
    Turk J Pediatr; 1991; 33(2):79-84. PubMed ID: 1844185
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Detection of parvovirus B19 DNA in amniotic fluid by PCR DNA amplification.
    Rogers BB; Mak SK; Dailey JV; Saller DN; Buffone GJ
    Biotechniques; 1993 Sep; 15(3):406-8, 410. PubMed ID: 8217152
    [No Abstract]   [Full Text] [Related]  

  • 26. Issues surrounding prenatal genetic testing for achondroplasia.
    Gooding HC; Boehm K; Thompson RE; Hadley D; Francomano CA; Biesecker BB
    Prenat Diagn; 2002 Oct; 22(10):933-40. PubMed ID: 12378581
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Prenatal echographic diagnosis of achondroplastic nanism].
    Caserta R; Zurzolo VS; Vagnetti P; Casolaro AM
    Minerva Ginecol; 1987; 39(7-8):533-6. PubMed ID: 3313117
    [No Abstract]   [Full Text] [Related]  

  • 28. First-trimester prenatal diagnosis in couple at risk for homozygous achondroplasia.
    Bellus GA; Escallon CS; Ortiz de Luna R; Shumway JB; Blakemore KJ; McIntosh I; Francomano CA
    Lancet; 1994 Nov; 344(8935):1511-2. PubMed ID: 7968151
    [No Abstract]   [Full Text] [Related]  

  • 29. [A new mutation causes achondrodysplasia. A simple DNA analysis confirms the diagnosis].
    Alderborn A; Anvret M; Gustavson KH; Hagenäs L; Wadelius C
    Lakartidningen; 1997 Jan; 94(5):341-2, 347. PubMed ID: 9053676
    [No Abstract]   [Full Text] [Related]  

  • 30. Feasibility of prenatal diagnosis of beta-thalassemia using two highly polymorphic microsatellites 5' to the beta-globin gene.
    Loudianos G; Cao A; Pirastu M
    Haematologica; 1992; 77(4):361-2. PubMed ID: 1427447
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pregnancy in an achondroplastic dwarf: a case report.
    Ghumman S; Goel N; Rajaram S; Singh KC; Kansal B; Dewan P
    J Indian Med Assoc; 2005 Oct; 103(10):536, 538. PubMed ID: 16498757
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Apert syndrome associated with increased fetal nuchal translucency.
    Aleem S; Howarth ES
    Prenat Diagn; 2005 Nov; 25(11):1066-7. PubMed ID: 16302163
    [No Abstract]   [Full Text] [Related]  

  • 33. Prenatal diagnosis and control strategies for beta-thalassaemia on the Indian subcontinent.
    Varawalla NY
    Natl Med J India; 1992; 5(4):157-61. PubMed ID: 1304300
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis of Apert syndrome.
    Chang CC; Tsai FJ; Tsai HD; Tsai CH; Hseih YY; Lee CC; Yang TC; Wu JY
    Prenat Diagn; 1998 Jun; 18(6):621-5. PubMed ID: 9664610
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recent progress in DNA technology.
    Mesci L; Gürgey A; Altay C
    Turk J Pediatr; 1993; 35(3):239-40. PubMed ID: 8165759
    [No Abstract]   [Full Text] [Related]  

  • 36. [Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
    Ezquieta Zubicaray B; Iguacel AO; Varela Junquera JM; Jariego Fente CM; González Gancedo P; Gracia Bouthelier R
    Med Clin (Barc); 1999 Mar; 112(8):290-3. PubMed ID: 10207844
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
    Chen P; Li MJ; Li MQ; Li SQ; Zhou LY; Lin WX
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(22):1540-4. PubMed ID: 17785106
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].
    Xu XM; Cai XH; Li J
    Zhonghua Yi Xue Za Zhi; 1994 Aug; 74(8):495-7, 520. PubMed ID: 7994662
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Achondroplasia: recent advances in diagnosis and treatment.
    Tanaka H
    Acta Paediatr Jpn; 1997 Aug; 39(4):514-20. PubMed ID: 9316303
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p.
    Francomano CA; Ortiz de Luna RI; Hefferon TW; Bellus GA; Turner CE; Taylor E; Meyers DA; Blanton SH; Murray JC; McIntosh I
    Hum Mol Genet; 1994 May; 3(5):787-92. PubMed ID: 8081365
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.