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64. Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Leppert M; Anderson VE; Quattlebaum T; Stauffer D; O'Connell P; Nakamura Y; Lalouel JM; White R Nature; 1989 Feb; 337(6208):647-8. PubMed ID: 2918897 [TBL] [Abstract][Full Text] [Related]
65. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A; Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740 [TBL] [Abstract][Full Text] [Related]
66. Evidence of a third locus for benign familial convulsions. Lewis TB; Shevell MI; Andermann E; Ryan SG; Leach RJ J Child Neurol; 1996 May; 11(3):211-4. PubMed ID: 8734025 [TBL] [Abstract][Full Text] [Related]
67. Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21. Schumacher J; König IR; Schröder T; Duell M; Plume E; Propping P; Warnke A; Libertus C; Ziegler A; Müller-Myhsok B; Schulte-Körne G; Nöthen MM Psychiatr Genet; 2008 Jun; 18(3):137-42. PubMed ID: 18496212 [TBL] [Abstract][Full Text] [Related]
68. Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred. Malik S; Schott J; Schiller J; Junge A; Baum E; Koch MC Eur J Hum Genet; 2008 Feb; 16(2):265-9. PubMed ID: 18000522 [TBL] [Abstract][Full Text] [Related]
69. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Holliday EG; McLean DE; Nyholt DR; Mowry BJ Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696 [TBL] [Abstract][Full Text] [Related]
70. [Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions]. Li HY; Tang BS; Yan XX; Guo JF; Shen L; Song YM; Jiang H; Xia K; Xie ZG; Yang QA Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):374-7. PubMed ID: 16883520 [TBL] [Abstract][Full Text] [Related]
71. Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1. Tomita Ha; Nagamitsu S; Wakui K; Fukushima Y; Yamada K; Sadamatsu M; Masui A; Konishi T; Matsuishi T; Aihara M; Shimizu K; Hashimoto K; Mineta M; Matsushima M; Tsujita T; Saito M; Tanaka H; Tsuji S; Takagi T; Nakamura Y; Nanko S; Kato N; Nakane Y; Niikawa N Am J Hum Genet; 1999 Dec; 65(6):1688-97. PubMed ID: 10577923 [TBL] [Abstract][Full Text] [Related]
72. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area. Shih WL; Yu MW; Chen PJ; Yeh SH; Lo MT; Chang HC; Liaw YF; Lin SM; Liu CJ; Lee SD; Lin CL; Hsiao CK; Yang SY; Chen CJ Oncogene; 2006 May; 25(22):3219-24. PubMed ID: 16407824 [TBL] [Abstract][Full Text] [Related]
73. [Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)]. Lefèvre A; Hiroz C; Zografos L; Schorderet DF; Munier FL Klin Monbl Augenheilkd; 1998 May; 212(5):301-4. PubMed ID: 9677562 [TBL] [Abstract][Full Text] [Related]
74. Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3. Azmanov DN; Zhelyazkova S; Radionova M; Morar B; Angelicheva D; Zlatareva D; Kaneva R; Tournev I; Kalaydjieva L; Sander JW Epilepsy Res; 2011 Sep; 96(1-2):101-8. PubMed ID: 21645995 [TBL] [Abstract][Full Text] [Related]
75. Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2. Scheffer IE; Phillips HA; O'Brien CE; Saling MM; Wrennall JA; Wallace RH; Mulley JC; Berkovic SF Ann Neurol; 1998 Dec; 44(6):890-9. PubMed ID: 9851433 [TBL] [Abstract][Full Text] [Related]
76. Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20. Sander T; Hildmann T; Wienker TF; Ramel C; Beck-Mannagetta G; Bianchi A; Sailer U; Berek K; Bauer G; Neitzel H; Schmitz B; Durner M; Johnson KJ; Janz D Am J Med Genet; 1996 Feb; 67(1):31-9. PubMed ID: 8678111 [TBL] [Abstract][Full Text] [Related]
77. Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene. Spacey SD; Valente EM; Wali GM; Warner TT; Jarman PR; Schapira AH; Dixon PH; Davis MB; Bhatia KP; Wood NW Mov Disord; 2002 Jul; 17(4):717-25. PubMed ID: 12210861 [TBL] [Abstract][Full Text] [Related]
79. A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype. Licchetta L; Pippucci T; Bisulli F; Cantalupo G; Magini P; Alvisi L; Baldassari S; Martinelli P; Naldi I; Vanni N; Liguori R; Seri M; Tinuper P Epilepsia; 2013 Jul; 54(7):1298-306. PubMed ID: 23663087 [TBL] [Abstract][Full Text] [Related]
80. Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family. Giordano L; Accorsi P; Valseriati D; Tiberti A; Menegati E; Zara F; Vignoli A; Vigevano F Neuropediatrics; 1999 Apr; 30(2):99-101. PubMed ID: 10401694 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]