250 related articles for article (PubMed ID: 18707033)
1. Clinical variability of the 22q11.2 duplication syndrome.
Wentzel C; Fernström M; Ohrner Y; Annerén G; Thuresson AC
Eur J Med Genet; 2008; 51(6):501-10. PubMed ID: 18707033
[TBL] [Abstract][Full Text] [Related]
2. Microduplication 22q11.2: a new chromosomal syndrome.
Portnoï MF
Eur J Med Genet; 2009; 52(2-3):88-93. PubMed ID: 19254783
[TBL] [Abstract][Full Text] [Related]
3. Concurrent microdeletion and duplication of 22q11.2.
Blennow E; Lagerstedt K; Malmgren H; Sahlén S; Schoumans J; Anderlid B
Clin Genet; 2008 Jul; 74(1):61-7. PubMed ID: 18445048
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo events.
Bi W; Probst FJ; Wiszniewska J; Plunkett K; Roney EK; Carter BS; Williams MD; Stankiewicz P; Patel A; Stevens CA; Lupski JR; Cheung SW
J Med Genet; 2012 Nov; 49(11):681-8. PubMed ID: 23042811
[TBL] [Abstract][Full Text] [Related]
6. Association of syndromic mental retardation and autism with 22q11.2 duplication.
Lo-Castro A; Galasso C; Cerminara C; El-Malhany N; Benedetti S; Nardone AM; Curatolo P
Neuropediatrics; 2009 Jun; 40(3):137-40. PubMed ID: 20020400
[TBL] [Abstract][Full Text] [Related]
7. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
[TBL] [Abstract][Full Text] [Related]
8. Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication.
Yu S; Cox K; Friend K; Smith S; Buchheim R; Bain S; Liebelt J; Thompson E; Bratkovic D
Clin Genet; 2008 Feb; 73(2):160-4. PubMed ID: 18076674
[TBL] [Abstract][Full Text] [Related]
9. Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.
Ramelli GP; Silacci C; Ferrarini A; Cattaneo C; Visconti P; Pescia G
Dev Med Child Neurol; 2008 Dec; 50(12):953-5. PubMed ID: 19046189
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment.
Lundin J; Söderhäll C; Lundén L; Hammarsjö A; White I; Schoumans J; Läckgren G; Kockum CC; Nordenskjöld A
Eur J Med Genet; 2010; 53(2):61-5. PubMed ID: 20045748
[TBL] [Abstract][Full Text] [Related]
12. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
[TBL] [Abstract][Full Text] [Related]
13. De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterization.
Lindsay EA; Shaffer LG; Carrozzo R; Greenberg F; Baldini A
Am J Med Genet; 1995 Apr; 56(3):296-9. PubMed ID: 7778594
[TBL] [Abstract][Full Text] [Related]
14. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
[TBL] [Abstract][Full Text] [Related]
15. Genetic background of congenital conotruncal heart defects--a study of 45 families.
Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
[TBL] [Abstract][Full Text] [Related]
16. Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
Draaken M; Reutter H; Schramm C; Bartels E; Boemers TM; Ebert AK; Rösch W; Schröder A; Stein R; Moebus S; Stienen D; Hoffmann P; Nöthen MM; Ludwig M
Eur J Med Genet; 2010; 53(2):55-60. PubMed ID: 20060941
[TBL] [Abstract][Full Text] [Related]
17. Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23.
Chang J; Zhao L; Chen C; Peng Y; Xia Y; Tang G; Bai T; Zhang Y; Ma R; Guo R; Mei L; Liang D; Cao Q; Wu L
Gene; 2015 Sep; 569(1):46-50. PubMed ID: 26099517
[TBL] [Abstract][Full Text] [Related]
18. [A study on the occurrence of the deletion 22q11.2 in patients affected with a psychiatric disease].
Pawłowska B; Tomankiewicz-Zawadzka A; Ilnicka A; Bogdanowicz J; Wciórka J; Szafrański T; Woźniak P; Meder J; Szaniawska-Bartnicka A; Zdzienicka E; Szirkowiec W; Zaremba J
Psychiatr Pol; 2007; 41(2):251-60. PubMed ID: 17598434
[TBL] [Abstract][Full Text] [Related]
19. Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.
De Smedt B; Swillen A; Verschaffel L; Ghesquière P
Dev Disabil Res Rev; 2009; 15(1):4-10. PubMed ID: 19213009
[TBL] [Abstract][Full Text] [Related]
20. Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations.
Shooner KA; Rope AF; Hopkin RJ; Andelfinger GU; Benson DW
J Pediatr; 2005 Mar; 146(3):382-7. PubMed ID: 15756225
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
