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.
1175 related articles for article (PubMed ID: 19239079)
21. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report. Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036 [TBL] [Abstract][Full Text] [Related]
22. Partial trisomy of the distal part of 10q: a report of two Egyptian cases. Aglan MS; Kamel AK; Helmy NA Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995 [TBL] [Abstract][Full Text] [Related]
23. Partial duplication of 4q12q13 leads to a mild phenotype. Shashi V; Berry MN; Santos C; Pettenati MJ Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828 [TBL] [Abstract][Full Text] [Related]
24. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion. Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767 [TBL] [Abstract][Full Text] [Related]
25. Autistic disorder and 22q11.2 duplication. Mukaddes NM; Herguner S World J Biol Psychiatry; 2007; 8(2):127-30. PubMed ID: 17455106 [TBL] [Abstract][Full Text] [Related]
26. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities]. Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216 [TBL] [Abstract][Full Text] [Related]
27. Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation. Koolen DA; Reardon W; Rosser EM; Lacombe D; Hurst JA; Law CJ; Bongers EM; van Ravenswaaij-Arts CM; Leisink MA; van Kessel AG; Veltman JA; de Vries BB Eur J Hum Genet; 2005 Sep; 13(9):1019-24. PubMed ID: 15986041 [TBL] [Abstract][Full Text] [Related]
28. A new case of a severe clinical phenotype of the cat-eye syndrome. Denavit TM; Malan V; Grillon C; Sanlaville D; Ardalan A; Jacquemont ML; Burglen L; Taillemite JL; Portnoi MF Genet Couns; 2004; 15(4):443-8. PubMed ID: 15658620 [TBL] [Abstract][Full Text] [Related]
29. A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephaly. Verhoeven W; Ruiter M; Egger J; Tuinier S; Smeets D Genet Couns; 2009; 20(1):45-51. PubMed ID: 19400541 [TBL] [Abstract][Full Text] [Related]
30. Duplication 6q syndrome. Tipton RE; Berns JS; Johnson WE; Wilroy RS; Summitt RL Am J Med Genet; 1979; 3(4):325-30. PubMed ID: 474632 [TBL] [Abstract][Full Text] [Related]
31. A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features. Hoffer MJ; Hilhorst-Hofstee Y; Knijnenburg J; Hansson KB; Engelberts AC; Laan LA; Bakker E; Rosenberg C Eur J Med Genet; 2007; 50(2):149-54. PubMed ID: 17223398 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features. Alberti A; Romano C; Falco M; Calì F; Schinocca P; Galesi O; Spalletta A; Di Benedetto D; Fichera M Clin Genet; 2007 Feb; 71(2):177-82. PubMed ID: 17250668 [TBL] [Abstract][Full Text] [Related]
34. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature. Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484 [TBL] [Abstract][Full Text] [Related]
35. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report. Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986 [TBL] [Abstract][Full Text] [Related]
36. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations. Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257 [TBL] [Abstract][Full Text] [Related]
37. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism. Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078 [TBL] [Abstract][Full Text] [Related]
38. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region. Tschernigg M; Petek E; Wagner K; Kroisel PM Genet Couns; 2002; 13(1):29-33. PubMed ID: 12017235 [TBL] [Abstract][Full Text] [Related]
39. Partial monosomy 11q and trisomy 12q: variable expression in two siblings. Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809 [TBL] [Abstract][Full Text] [Related]
40. De novo trisomy 22 due to an extra 22Q-chromosome. Stoll C; Medeiros P; Pécheur H; Schnebelen A Ann Genet; 1997; 40(4):217-21. PubMed ID: 9526616 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]