BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 36672887)

  • 21. Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.
    Di Bartolo DL; El Naggar M; Owen R; Sahoo T; Gilbert F; Pulijaal VR; Mathew S
    Mol Cytogenet; 2012 Jul; 5(1):31. PubMed ID: 22768875
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Pure distal 9p deletion in a female infant with cerebral palsy.
    Chen CP; Lin SP; Su YN; Su JW; Chern SR; Town DD; Wang W
    Genet Couns; 2012; 23(2):215-21. PubMed ID: 22876580
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The 9p-syndrome.
    Funderburk SJ; Sparkes RS; Klisak I
    J Med Genet; 1979 Feb; 16(1):75-9. PubMed ID: 469892
    [TBL] [Abstract][Full Text] [Related]  

  • 24. CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features.
    Jyonouchi S; McDonald-McGinn DM; Bale S; Zackai EH; Sullivan KE
    Pediatrics; 2009 May; 123(5):e871-7. PubMed ID: 19403480
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
    McDonald-McGinn DM; Tonnesen MK; Laufer-Cahana A; Finucane B; Driscoll DA; Emanuel BS; Zackai EH
    Genet Med; 2001; 3(1):23-9. PubMed ID: 11339373
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.
    Jelin A; Perry H; Hogue J; Oberoi S; Cotter PD; Klein OD
    J Craniofac Surg; 2010 Sep; 21(5):1376-9. PubMed ID: 20856024
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Smith-Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature.
    Onesimo R; Versacci P; Delogu AB; De Rosa G; Pugnaloni F; Blandino R; Leoni C; Calcagni G; Digilio MC; Zollino M; Marino B; Zampino G
    Am J Med Genet A; 2021 Jul; 185(7):2003-2011. PubMed ID: 33811726
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.
    Quélin C; Bendavid C; Dubourg C; de la Rochebrochard C; Lucas J; Henry C; Jaillard S; Loget P; Loeuillet L; Lacombe D; Rival JM; David V; Odent S; Pasquier L
    Eur J Med Genet; 2009; 52(1):41-6. PubMed ID: 19022413
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [9p-syndrome].
    Fujita H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):318-9. PubMed ID: 11057244
    [No Abstract]   [Full Text] [Related]  

  • 32. Ring chromosome 9 in a girl with developmental delay and dysmorphic features: case report and review of the literature.
    la Cour Sibbesen E; Jespersgaard C; Alosi D; Bisgaard AM; Tümer Z
    Am J Med Genet A; 2013 Jun; 161A(6):1447-52. PubMed ID: 23633410
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion.
    Neira VA; Córdova-Fletes C; Grondin Y; Ramirez-Velazco A; Figuera LE; Ortíz-López R; Barbaro M
    Am J Med Genet A; 2012 Jun; 158A(6):1498-502. PubMed ID: 22581498
    [No Abstract]   [Full Text] [Related]  

  • 34. Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations.
    Sirisena ND; Wijetunge UK; de Silva R; Dissanayake VH
    Case Rep Genet; 2013; 2013():785830. PubMed ID: 23984121
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation.
    Tayel SM; Kurczynski TW; Casperson S; McCorquodale MM
    Am J Med Genet; 1988 Dec; 31(4):853-61. PubMed ID: 3239578
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome.
    Bayat A; Kirchhoff M; Madsen CG; Kreiborg S
    Eur J Med Genet; 2018 Aug; 61(8):473-477. PubMed ID: 29601900
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease.
    Putotto C; Unolt M; Lambiase C; Marchetti F; Anaclerio S; Favoriti A; Tancredi G; Mastromoro G; Pugnaloni F; Liberati N; De Luca E; Tarani L; De Canditiis D; Caputo V; Bernardini L; Digilio MC; Marino B; Versacci P
    Eur J Med Genet; 2023 Jan; 66(1):104651. PubMed ID: 36404488
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 3p14 deletion is a rare contiguous gene syndrome: report of 2 new patients and an overview of 14 patients.
    Dimitrov BI; Ogilvie C; Wieczorek D; Wakeling E; Sikkema-Raddatz B; van Ravenswaaij-Arts CM; Josifova D
    Am J Med Genet A; 2015 Jun; 167(6):1223-30. PubMed ID: 25908055
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
    Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
    Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
    De Backer J
    Verh K Acad Geneeskd Belg; 2009; 71(6):335-71. PubMed ID: 20232788
    [TBL] [Abstract][Full Text] [Related]  

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