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.
123 related articles for article (PubMed ID: 12567408)
1. Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus. Petek E; Windpassinger C; Mach M; Rauter L; Scherer SW; Wagner K; Kroisel PM Am J Med Genet A; 2003 Mar; 117A(2):122-6. PubMed ID: 12567408 [TBL] [Abstract][Full Text] [Related]
2. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. Greene CC; McMillan PM; Barker SE; Kurnool P; Lomax MI; Burmeister M; Lesperance MM Am J Hum Genet; 2001 Jan; 68(1):254-60. PubMed ID: 11115382 [TBL] [Abstract][Full Text] [Related]
3. A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter. Blanton SH; Liang CY; Cai MW; Pandya A; Du LL; Landa B; Mummalanni S; Li KS; Chen ZY; Qin XN; Liu YF; Balkany T; Nance WE; Liu XZ J Med Genet; 2002 Aug; 39(8):567-70. PubMed ID: 12161595 [TBL] [Abstract][Full Text] [Related]
4. Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. Petek E; Windpassinger C; Simma B; Mueller T; Wagner K; Kroisel PM J Hum Genet; 2003; 48(6):283-287. PubMed ID: 12836054 [TBL] [Abstract][Full Text] [Related]
5. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. Mangino M; Flex E; Capon F; Sangiuolo F; Carraro E; Gualandi F; Mazzoli M; Martini A; Novelli G; Dallapiccola B Eur J Hum Genet; 2001 Sep; 9(9):667-71. PubMed ID: 11571554 [TBL] [Abstract][Full Text] [Related]
6. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p). Baens M; Wlodarska I; Corveleyn A; Hoornaert I; Hagemeijer A; Marynen P Genomics; 1999 Feb; 56(1):40-50. PubMed ID: 10036184 [TBL] [Abstract][Full Text] [Related]
7. Physical mapping of a commonly deleted region, the site of a candidate tumor suppressor gene, at 12q22 in human male germ cell tumors. Murty VV; Renault B; Falk CT; Bosl GJ; Kucherlapati R; Chaganti RS Genomics; 1996 Aug; 35(3):562-70. PubMed ID: 8812492 [TBL] [Abstract][Full Text] [Related]
8. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q. Kumar S; Kimberling WJ; Lanyi A; Sumegi J; Pinnt J; Ing P; Tinley S; Marres HA; Cremers CW Genomics; 1996 Jan; 31(1):71-9. PubMed ID: 8808282 [TBL] [Abstract][Full Text] [Related]
9. Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene. Ofner L; Raedle J; Windpassinger C; Schwarzbraun T; Kroisel PM; Wagner K; Petek E J Hum Genet; 2006; 51(2):141-146. PubMed ID: 16365682 [TBL] [Abstract][Full Text] [Related]
10. Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. Masmoudi S; Tlili A; Majava M; Ghorbel AM; Chardenoux S; Lemainque A; Zina ZB; Moala J; Männikkö M; Weil D; Lathrop M; Ala-Kokko L; Drira M; Petit C; Ayadi H Eur J Hum Genet; 2003 Feb; 11(2):185-8. PubMed ID: 12634867 [TBL] [Abstract][Full Text] [Related]
11. A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3. Aslam M; Wajid M; Chahrour MH; Ansar M; Haque S; Pham TL; Santos RP; Yan K; Ahmad W; Leal SM Am J Med Genet A; 2005 Feb; 133A(1):18-22. PubMed ID: 15641023 [TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl. Kumar A; Cassidy SB; Romero L; Schwartz S Am J Med Genet; 1999 Sep; 86(3):227-31. PubMed ID: 10482870 [TBL] [Abstract][Full Text] [Related]
13. DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15. Waryah AM; Rehman A; Ahmed ZM; Bashir ZH; Khan SY; Zafar AU; Riazuddin S; Friedman TB; Riazuddin S Clin Genet; 2009 Sep; 76(3):270-5. PubMed ID: 19650862 [TBL] [Abstract][Full Text] [Related]
14. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene. Irobi J; Tissir F; De Jonghe P; De Vriendt E; Van Broeckhoven C; Timmerman V; Beuten J Genomics; 2000 Apr; 65(1):34-43. PubMed ID: 10777663 [TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation. Wester U; Bondeson ML; Edeby C; Annerén G Am J Med Genet A; 2006 Jun; 140(11):1164-71. PubMed ID: 16691587 [TBL] [Abstract][Full Text] [Related]
16. [Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)]. Sun HJ; Tao R; Cheng J; Yang SZ; Cao JY; Yu LM; Hong MD; Feng GY; Dai P; Yuan HJ; Han DY; He L Yi Chuan; 2006 Dec; 28(12):1489-94. PubMed ID: 17138532 [TBL] [Abstract][Full Text] [Related]
17. Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences. Barber JC; Maloney VK; Kirchhoff M; Thomas NS; Boyle TA; Castle B Am J Med Genet A; 2007 Mar; 143A(6):615-8. PubMed ID: 17318843 [No Abstract] [Full Text] [Related]
18. Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours. Perotti D; Testi MA; Mondini P; Pilotti S; Green ED; Pession A; Sozzi G; Pierotti MA; Fossati-Bellani F; Radice P Genes Chromosomes Cancer; 2001 May; 31(1):42-7. PubMed ID: 11284034 [TBL] [Abstract][Full Text] [Related]
19. A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4. Kalay E; Caylan R; Kiroglu AF; Yasar T; Collin RW; Heister JG; Oostrik J; Cremers CW; Brunner HG; Karaguzel A; Kremer H J Mol Med (Berl); 2007 Apr; 85(4):397-404. PubMed ID: 17211611 [TBL] [Abstract][Full Text] [Related]
20. Characterization of a t(10;12)(q24;p13) in a case of CML in transformation. Aguiar RC; Chase A; Oscier DG; Carapeti M; Goldman JM; Cross NC Genes Chromosomes Cancer; 1997 Dec; 20(4):408-11. PubMed ID: 9408758 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]