271 related articles for article (PubMed ID: 22555022)
1. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.
Yang Y; Wang C; Wang F; Zhu L; Liu H; He X
Gene; 2012 Jul; 502(2):154-8. PubMed ID: 22555022
[TBL] [Abstract][Full Text] [Related]
2. A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
Abu-Amero KK; Hellani AM; Salih MA; Seidahmed MZ; Elmalik TS; Zidan G; Bosley TM
BMC Med Genet; 2010 Sep; 11():135. PubMed ID: 20858261
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
[TBL] [Abstract][Full Text] [Related]
5. Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.
Bonnet C; Grégoire MJ; Vibert M; Raffo E; Leheup B; Jonveaux P
J Hum Genet; 2008; 53(10):876-885. PubMed ID: 18651096
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
[TBL] [Abstract][Full Text] [Related]
7. Identification and molecular characterization of two novel chromosomal deletions associated with autism.
Chien WH; Gau SS; Wu YY; Huang YS; Fang JS; Chen YJ; Soong WT; Chiu YN; Chen CH
Clin Genet; 2010 Nov; 78(5):449-56. PubMed ID: 20236125
[TBL] [Abstract][Full Text] [Related]
8. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
9. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
[TBL] [Abstract][Full Text] [Related]
10. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
[TBL] [Abstract][Full Text] [Related]
11. Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.
Hoo JJ; Fischer A; Fuhrmann W
Ann Genet; 1982; 25(4):249-52. PubMed ID: 6985017
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Association of deletion 9p, 46,XY gonadal dysgenesis and autistic spectrum disorder.
Vinci G; Chantot-Bastaraud S; El Houate B; Lortat-Jacob S; Brauner R; McElreavey K
Mol Hum Reprod; 2007 Sep; 13(9):685-9. PubMed ID: 17644778
[TBL] [Abstract][Full Text] [Related]
14. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
[TBL] [Abstract][Full Text] [Related]
15. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
16. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G
Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338
[TBL] [Abstract][Full Text] [Related]
17. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
Peters SU; Horowitz L; Barbieri-Welge R; Taylor JL; Hundley RJ
J Child Psychol Psychiatry; 2012 Feb; 53(2):152-9. PubMed ID: 21831244
[TBL] [Abstract][Full Text] [Related]
18. Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.
Nguyen-Minh S; Drossel K; Horn D; Rost I; Spors B; Kaindl AM
Gene; 2013 Jul; 523(1):92-8. PubMed ID: 23566840
[TBL] [Abstract][Full Text] [Related]
19. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
Wagstaff J; Hemann M
Am J Hum Genet; 1995 Jan; 56(1):302-9. PubMed ID: 7825591
[TBL] [Abstract][Full Text] [Related]
20. A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
Mohrschladt MF; Bijlsma EK; Sluijter S; De Coo RF; Hoovers JM; Leschot NJ
Clin Dysmorphol; 1999 Jul; 8(3):211-4. PubMed ID: 10457857
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
