145 related articles for article (PubMed ID: 9152831)
1. The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.
Arnell H; Hjälmås K; Jägervall M; Läckgren G; Stenberg A; Bengtsson B; Wassén C; Emahazion T; Annerén G; Pettersson U; Sundvall M; Dahl N
J Med Genet; 1997 May; 34(5):360-5. PubMed ID: 9152831
[TBL] [Abstract][Full Text] [Related]
2. Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q.
Eiberg H; Berendt I; Mohr J
Nat Genet; 1995 Jul; 10(3):354-6. PubMed ID: 7670476
[TBL] [Abstract][Full Text] [Related]
3. Does monosymptomatic enuresis exist? A molecular genetic exploration of 32 families with enuresis/incontinence.
Loeys B; Hoebeke P; Raes A; Messiaen L; De Paepe A; Vande Walle J
BJU Int; 2002 Jul; 90(1):76-83. PubMed ID: 12081775
[TBL] [Abstract][Full Text] [Related]
4. The aquaporin-2 water channel in autosomal dominant primary nocturnal enuresis.
Deen PM; Dahl N; Caplan MJ
J Urol; 2002 Mar; 167(3):1447-50. PubMed ID: 11832768
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetics of nocturnal enuresis: clinical and genetic heterogeneity.
von Gontard A; Eiberg H; Hollmann E; Rittig S; Lehmkuhl G
Acta Paediatr; 1998 May; 87(5):571-8. PubMed ID: 9641742
[TBL] [Abstract][Full Text] [Related]
6. Molecular genetics of nocturnal enuresis: linkage to a locus on chromosome 22.
von Gontard A; Eiberg H; Hollmann E; Rittig S; Lehmkuhl G
Scand J Urol Nephrol Suppl; 1999; 202():76-80. PubMed ID: 10573802
[TBL] [Abstract][Full Text] [Related]
7. Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.
Desautels A; Turecki G; Montplaisir J; Xiong L; Walters AS; Ehrenberg BL; Brisebois K; Desautels AK; Gingras Y; Johnson WG; Lugaresi E; Coccagna G; Picchietti DL; Lazzarini A; Rouleau GA
Arch Neurol; 2005 Apr; 62(4):591-6. PubMed ID: 15824258
[TBL] [Abstract][Full Text] [Related]
8. Total genome scan analysis in a single extended family for primary nocturnal enuresis: evidence for a new locus (ENUR3) for primary nocturnal enuresis on chromosome 22q11.
Eiberg H
Eur Urol; 1998; 33 Suppl 3():34-6. PubMed ID: 9599735
[TBL] [Abstract][Full Text] [Related]
9. The genetic basis of inherited primary nocturnal enuresis: A UAE study.
Bayoumi RA; Eapen V; Al-Yahyaee S; Al Barwani HS; Hill RS; Al Gazali L
J Psychosom Res; 2006 Sep; 61(3):317-20. PubMed ID: 16938508
[TBL] [Abstract][Full Text] [Related]
10. Linkage study of a large Danish 4-generation family with urge incontinence and nocturnal enuresis.
Eiberg H; Shaumburg HL; Von Gontard A; Rittig S
J Urol; 2001 Dec; 166(6):2401-3. PubMed ID: 11696797
[TBL] [Abstract][Full Text] [Related]
11. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
[TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
[TBL] [Abstract][Full Text] [Related]
13. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
14. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
[TBL] [Abstract][Full Text] [Related]
15. Transmission of primary nocturnal enuresis and attention deficit hyperactivity disorder.
Bailey JN; Ornitz EM; Gehricke JG; Gabikian P; Russell AT; Smalley SL
Acta Paediatr; 1999 Dec; 88(12):1364-8. PubMed ID: 10626523
[TBL] [Abstract][Full Text] [Related]
16. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
[TBL] [Abstract][Full Text] [Related]
17. Family and segregation studies: 411 Chinese children with primary nocturnal enuresis.
Wang QW; Wen JG; Zhang RL; Yang HY; Su J; Liu K; Zhu QH; Zhang P
Pediatr Int; 2007 Oct; 49(5):618-22. PubMed ID: 17875087
[TBL] [Abstract][Full Text] [Related]
18. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
19. Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
Rogaeva E; Premkumar S; Song Y; Sorbi S; Brindle N; Paterson A; Duara R; Levesque G; Yu G; Nishimura M; Ikeda M; O'Toole C; Kawarai T; Jorge R; Vilarino D; Bruni AC; Farrer LA; St George-Hyslop PH
JAMA; 1998 Aug; 280(7):614-8. PubMed ID: 9718052
[TBL] [Abstract][Full Text] [Related]
20. Familial cavitary optic disk anomalies: identification of a novel genetic locus.
Fingert JH; Honkanen RA; Shankar SP; Affatigato LM; Ehlinger MA; Moore MD; Jampol LM; Sheffield VC; Stone EM; Alward WL
Am J Ophthalmol; 2007 May; 143(5):795-800. PubMed ID: 17368552
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]