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5. 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay. Cusmano-Ozog K; Manning MA; Hoyme HE Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):393-8. PubMed ID: 17926345 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome). Sarasua SM; Dwivedi A; Boccuto L; Rollins JD; Chen CF; Rogers RC; Phelan K; DuPont BR; Collins JS J Med Genet; 2011 Nov; 48(11):761-6. PubMed ID: 21984749 [TBL] [Abstract][Full Text] [Related]
9. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. Zollino M; Di Stefano C; Zampino G; Mastroiacovo P; Wright TJ; Sorge G; Selicorni A; Tenconi R; Zappalà A; Battaglia A; Di Rocco M; Palka G; Pallotta R; Altherr MR; Neri G Am J Med Genet; 2000 Sep; 94(3):254-61. PubMed ID: 10995514 [TBL] [Abstract][Full Text] [Related]
10. Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3. Delahaye A; Toutain A; Aboura A; Dupont C; Tabet AC; Benzacken B; Elion J; Verloes A; Pipiras E; Drunat S Eur J Med Genet; 2009; 52(5):328-32. PubMed ID: 19454329 [TBL] [Abstract][Full Text] [Related]
14. Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardation. Ligon AH; Beaudet AL; Shaffer LG Am J Hum Genet; 1997 Jul; 61(1):51-9. PubMed ID: 9245984 [TBL] [Abstract][Full Text] [Related]
15. Deletion mapping by FISH with BACs in patients with partial monosomy 22q13. Schröder K; Schuffenhauer S; Seidel H; Bartsch O; Blin N; Hinkel GK; Schmitt H Hum Genet; 1998 May; 102(5):557-61. PubMed ID: 9654204 [TBL] [Abstract][Full Text] [Related]
16. [Clinical phenotypes and genetic study of 2 cases with 22q13 deletion syndrome]. Luo J; Fang D; Qiu W; Xiao B; Fan Y; Ye J; Han L; Zhang H; Yu Y; Liang L; Gu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):361-365. PubMed ID: 29896732 [TBL] [Abstract][Full Text] [Related]
17. Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms. Wilson HL; Wong AC; Shaw SR; Tse WY; Stapleton GA; Phelan MC; Hu S; Marshall J; McDermid HE J Med Genet; 2003 Aug; 40(8):575-84. PubMed ID: 12920066 [TBL] [Abstract][Full Text] [Related]
18. Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22. Battini R; Battaglia A; Bertini V; Cioni G; Parrini B; Rapalini E; Simi P; Tinelli F; Valetto A Am J Med Genet A; 2004 Oct; 130A(2):196-9. PubMed ID: 15372517 [TBL] [Abstract][Full Text] [Related]
19. 22q13 deletion syndrome with central diabetes insipidus: a previously unreported association. Barakat AJ; Pearl PL; Acosta MT; Runkle BP Clin Dysmorphol; 2004 Jul; 13(3):191-194. PubMed ID: 15194959 [TBL] [Abstract][Full Text] [Related]
20. Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood. Philippe A; Boddaert N; Vaivre-Douret L; Robel L; Danon-Boileau L; Malan V; de Blois MC; Heron D; Colleaux L; Golse B; Zilbovicius M; Munnich A Pediatrics; 2008 Aug; 122(2):e376-82. PubMed ID: 18625665 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]