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 *

174 related articles for article (PubMed ID: 34132911)

  • 21. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A new case of 8q22.1 microdeletion restricts the critical region for Nablus mask-like facial syndrome.
    Debost-Legrand A; Eymard-Pierre E; Pebrel-Richard C; Gouas L; Goumy C; Giollant M; Ayed W; Tchirkov A; Francannet C; Vago P
    Am J Med Genet A; 2013 Jan; 161A(1):162-5. PubMed ID: 23239647
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
    Shimojima K; Páez MT; Kurosawa K; Yamamoto T
    Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.
    Klopocki E; Graul-Neumann LM; Grieben U; Tönnies H; Ropers HH; Horn D; Mundlos S; Ullmann R
    Eur J Pediatr; 2008 Aug; 167(8):903-8. PubMed ID: 17932688
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
    Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
    Wang HD; Liu L; Wu D; Li T; Cui CY; Zhang LZ; Wang CZ
    J Gene Med; 2017 Apr; 19(4):. PubMed ID: 28220983
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
    Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
    Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
    Bonnet C; Andrieux J; Béri-Dexheimer M; Leheup B; Boute O; Manouvrier S; Delobel B; Copin H; Receveur A; Mathieu M; Thiriez G; Le Caignec C; David A; de Blois MC; Malan V; Philippe A; Cormier-Daire V; Colleaux L; Flori E; Dollfus H; Pelletier V; Thauvin-Robinet C; Masurel-Paulet A; Faivre L; Tardieu M; Bahi-Buisson N; Callier P; Mugneret F; Edery P; Jonveaux P; Sanlaville D
    J Med Genet; 2010 Jun; 47(6):377-84. PubMed ID: 20522426
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 2q24 deletions: further characterization of clinical findings and their relation to the SCN cluster.
    Nimmakayalu M; Noble N; Horton VK; Willing M; Copeland S; Sheffield V; Nagy PL; Wassink T; Patil S; Shchelochkov OA
    Am J Med Genet A; 2012 Nov; 158A(11):2767-74. PubMed ID: 23023937
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Delineation of the proximal 3q microdeletion syndrome.
    Simovich MJ; Bland SD; Peiffer DA; Gunderson KL; Cheung SW; Yatsenko SA; Shinawi M
    Am J Med Genet A; 2008 Jul; 146A(13):1729-35. PubMed ID: 18536049
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions.
    Bensaid S; Bendahmane M; Loddo S; Poke G; Januel L; Nicolle R; Malan V; Chatron N; Ottombrino S; Dentici ML; Novelli A; Digilio MC; Sanlaville D
    Am J Med Genet A; 2024 Jul; 194(7):e63580. PubMed ID: 38511524
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome.
    Filges I; Röthlisberger B; Boesch N; Weber P; Wenzel F; Huber AR; Heinimann K; Miny P
    Am J Med Genet A; 2010 Apr; 152A(4):987-93. PubMed ID: 20358614
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Adult expression of a 3q13.31 microdeletion.
    Lowther C; Costain G; Melvin R; Stavropoulos DJ; Lionel AC; Marshall CR; Scherer SW; Bassett AS
    Mol Cytogenet; 2014 Mar; 7(1):23. PubMed ID: 24650298
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Five patients with novel overlapping interstitial deletions in 8q22.2q22.3.
    Kuechler A; Buysse K; Clayton-Smith J; Le Caignec C; David A; Engels H; Kohlhase J; Mari F; Mortier G; Renieri A; Wieczorek D
    Am J Med Genet A; 2011 Aug; 155A(8):1857-64. PubMed ID: 21739578
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles.
    Serra G; Antona V; Giuffrè M; Piro E; Salerno S; Schierz IAM; Corsello G
    Ital J Pediatr; 2022 Mar; 48(1):38. PubMed ID: 35246213
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
    Willemsen MH; Fernandez BA; Bacino CA; Gerkes E; de Brouwer AP; Pfundt R; Sikkema-Raddatz B; Scherer SW; Marshall CR; Potocki L; van Bokhoven H; Kleefstra T
    Eur J Hum Genet; 2010 Apr; 18(4):429-35. PubMed ID: 19920853
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.
    Piccione M; Piro E; Serraino F; Cavani S; Ciccone R; Malacarne M; Pierluigi M; Vitaloni M; Zuffardi O; Corsello G
    Eur J Med Genet; 2012 Apr; 55(4):238-44. PubMed ID: 22406401
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic features of a microdeletion in chromosome band 20p13: A case report and review of the literature.
    Fang HH; Liu SY; Wang YF; Chiang CM; Liu CC; Lin CM
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00739. PubMed ID: 31087544
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
    Nagamani SC; Erez A; Eng C; Ou Z; Chinault C; Workman L; Coldwell J; Stankiewicz P; Patel A; Lupski JR; Cheung SW
    Eur J Hum Genet; 2009 May; 17(5):573-81. PubMed ID: 19034313
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.