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.
168 related articles for article (PubMed ID: 19233321)
1. Congenital diaphragmatic hernia is part of the new 15q24 microdeletion syndrome. Van Esch H; Backx L; Pijkels E; Fryns JP Eur J Med Genet; 2009; 52(2-3):153-6. PubMed ID: 19233321 [TBL] [Abstract][Full Text] [Related]
2. 15q24.1 BP4-BP1 microdeletion unmasking paternally inherited functional polymorphisms combined with distal 15q24.2q24.3 duplication in a patient with epilepsy, psychomotor delay, overweight, ventricular arrhythmia. Huynh MT; Lambert AS; Tosca L; Petit F; Philippe C; Parisot F; Benoît V; Linglart A; Brisset S; Tran CT; Tachdjian G; Receveur A Eur J Med Genet; 2018 Aug; 61(8):459-464. PubMed ID: 29549028 [TBL] [Abstract][Full Text] [Related]
4. Kidney abnormalities in persons with monosomy 15q26. Lurie IW Am J Med Genet A; 2008 Jul; 146A(13):1761-4. PubMed ID: 18512227 [No Abstract] [Full Text] [Related]
5. 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]
6. Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review. Liu Y; Mapow B Mol Genet Genomic Med; 2020 Jul; 8(7):e1265. PubMed ID: 32400031 [TBL] [Abstract][Full Text] [Related]
7. Refining critical regions in 15q24 microdeletion syndrome pertaining to autism. Liu Y; Zhang Y; Zarrei M; Dong R; Yang X; Zhao D; Scherer SW; Gai Z Am J Med Genet B Neuropsychiatr Genet; 2020 Jun; 183(4):217-226. PubMed ID: 31953991 [TBL] [Abstract][Full Text] [Related]
8. Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia. van Dooren MF; Brooks AS; Hoogeboom AJ; van den Hoonaard TL; de Klein JE; Wouters CH; Tibboel D Am J Med Genet A; 2004 Jun; 127A(2):194-6. PubMed ID: 15108210 [TBL] [Abstract][Full Text] [Related]
15. An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature. L Ng IS; Chin WH; P Lim EC; Tan EC Twin Res Hum Genet; 2011 Aug; 14(4):333-9. PubMed ID: 21787116 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci. Doelken SC; Seeger K; Hundsdoerfer P; Weber-Ferro W; Klopocki E; Graul-Neumann L Am J Med Genet A; 2013 Jan; 161A(1):218-24. PubMed ID: 23239641 [TBL] [Abstract][Full Text] [Related]
18. Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature. Hengstschläger M; Mittermayer C; Repa C; Drahonsky R; Deutinger J; Bernaschek G Fetal Diagn Ther; 2004; 19(6):510-2. PubMed ID: 15539876 [TBL] [Abstract][Full Text] [Related]
19. New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome. Rosenfeld JA; Lacassie Y; El-Khechen D; Escobar LF; Reggin J; Heuer C; Chen E; Jenkins LS; Collins AT; Zinner S; Babcock M; Morrow B; Schultz RA; Torchia BS; Ballif BC; Tsuchiya KD; Shaffer LG Eur J Med Genet; 2011; 54(1):42-9. PubMed ID: 20951845 [TBL] [Abstract][Full Text] [Related]