145 related articles for article (PubMed ID: 16826529)
1. Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16p12-p13 and evidence for genetic heterogeneity.
Capon F; Reece A; Ravindrarajah R; Chung E
Am J Hum Genet; 2006 Aug; 79(2):378-82. PubMed ID: 16826529
[TBL] [Abstract][Full Text] [Related]
2. Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24.
Everett KV; Capon F; Georgoula C; Chioza BA; Reece A; Jaswon M; Pierro A; Puri P; Gardiner RM; Chung EM
Eur J Hum Genet; 2008 Sep; 16(9):1151-4. PubMed ID: 18478043
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23.
Everett KV; Chioza BA; Georgoula C; Reece A; Capon F; Parker KA; Cord-Udy C; McKeigue P; Mitton S; Pierro A; Puri P; Mitchison HM; Chung EM; Gardiner RM
Am J Hum Genet; 2008 Mar; 82(3):756-62. PubMed ID: 18308288
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.
Svenningsson A; Söderhäll C; Persson S; Lundberg F; Luthman H; Chung E; Gardiner M; Kockum I; Nordenskjöld A
J Hum Genet; 2012 Feb; 57(2):115-21. PubMed ID: 22158425
[TBL] [Abstract][Full Text] [Related]
5. Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing.
Everett KV; Chioza BA; Georgoula C; Reece A; Gardiner RM; Chung EM
Hum Genet; 2009 Dec; 126(6):819-31. PubMed ID: 19701773
[TBL] [Abstract][Full Text] [Related]
6. Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5.
Everett KV; Chung EM
J Hum Genet; 2013 Apr; 58(4):236-7. PubMed ID: 23426030
[TBL] [Abstract][Full Text] [Related]
7. Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
Feenstra B; Geller F; Carstensen L; Romitti PA; Körberg IB; Bedell B; Krogh C; Fan R; Svenningsson A; Caggana M; Nordenskjöld A; Mills JL; Murray JC; Melbye M
JAMA; 2013 Aug; 310(7):714-21. PubMed ID: 23989729
[TBL] [Abstract][Full Text] [Related]
8. A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24.
Everett KV; Ataliotis P; Chioza BA; Shaw-Smith C; Chung EMK
Pediatr Res; 2017 Apr; 81(4):632-638. PubMed ID: 27855150
[TBL] [Abstract][Full Text] [Related]
9. Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.
Disse S; Abergel E; Berrebi A; Houot AM; Le Heuzey JY; Diebold B; Guize L; Carpentier A; Corvol P; Jeunemaitre X
Am J Hum Genet; 1999 Nov; 65(5):1242-51. PubMed ID: 10521289
[TBL] [Abstract][Full Text] [Related]
10. No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis.
Lagerstedt-Robinson K; Svenningsson A; Nordenskjöld A
J Hum Genet; 2009 Dec; 54(12):706-8. PubMed ID: 19851341
[TBL] [Abstract][Full Text] [Related]
11. Linkage analysis of infantile pyloric stenosis and markers from chromosome 9q11-q33: no evidence for a major gene in this candidate region.
Chung E; Coffey R; Parker K; Tam P; Pembrey ME; Gardiner RM
J Med Genet; 1993 May; 30(5):393-5. PubMed ID: 8320701
[TBL] [Abstract][Full Text] [Related]
12. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion].
Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW
Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426
[TBL] [Abstract][Full Text] [Related]
13. Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family.
Lee WL; Tay A; Ong HT; Goh LM; Monaco AP; Szepetowski P
Hum Genet; 1998 Nov; 103(5):608-12. PubMed ID: 9860304
[TBL] [Abstract][Full Text] [Related]
14. Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13.
Weiss MJ; Guo C; Shusterman S; Hii G; Mirensky TL; White PS; Hogarty MD; Rebbeck TR; Teare D; Urbanek M; Brodeur GM; Maris JM
Med Pediatr Oncol; 2000 Dec; 35(6):526-30. PubMed ID: 11107108
[TBL] [Abstract][Full Text] [Related]
15. Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Caraballo R; Pavek S; Lemainque A; Gastaldi M; Echenne B; Motte J; Genton P; Cersósimo R; Humbertclaude V; Fejerman N; Monaco AP; Lathrop MG; Rochette J; Szepetowski P
Am J Hum Genet; 2001 Mar; 68(3):788-94. PubMed ID: 11179027
[TBL] [Abstract][Full Text] [Related]
16. Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.
Hateboer N; Gumbs C; Teare MD; Coles GA; Griffiths D; Ravine D; Futreal PA; Rahman N
Kidney Int; 2001 Oct; 60(4):1233-9. PubMed ID: 11576337
[TBL] [Abstract][Full Text] [Related]
17. Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.
Striano P; Lispi ML; Gennaro E; Madia F; Traverso M; Bordo L; Aridon P; Martinelli Boneschi F; Barone B; dalla Bernardina B; Bianchi A; Capovilla G; De Marco P; Dulac O; Gaggero R; Gambardella A; Nabbout R; Prud'homme JF; Day R; Vanadia F; Vecchi M; Veggiotti P; Vigevano F; Viri M; Minetti C; Zara F
Epilepsia; 2006 Jun; 47(6):1029-34. PubMed ID: 16822249
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family.
de Almeida S; de Almeida E; Peters D; Pinto JR; Távora I; Lavinha J; Breuning M; Prata MM
Hum Genet; 1995 Jul; 96(1):83-8. PubMed ID: 7607660
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
Fadista J; Skotte L; Geller F; Bybjerg-Grauholm J; Gørtz S; Romitti PA; Caggana M; Kay DM; Matsson H; Boyd HA; Hougaard DM; Nordenskjöld A; Mills JL; Melbye M; Feenstra B
Hum Mol Genet; 2019 Jan; 28(2):332-340. PubMed ID: 30281099
[TBL] [Abstract][Full Text] [Related]
20. Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13.
Stacey JM; Turner JJ; Harding B; Nesbit MA; Kotanko P; Lhotta K; Puig JG; Torres RJ; Thakker RV
J Clin Endocrinol Metab; 2003 Jan; 88(1):464-70. PubMed ID: 12519891
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
