Kong X, Bousfiha A, Rouissi A, Itan Y, Abhyankar A, Bryant V
PLoS One. 2013; 8(3):e58286.
PMID: 23472171
PMC: 3589270.
DOI: 10.1371/journal.pone.0058286.
Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P
Invest Ophthalmol Vis Sci. 2011; 52(9):6814-9.
PMID: 21357393
PMC: 3176007.
DOI: 10.1167/iovs.10-6815.
Jun G, Song Y, Iyengar S, Elston R
BMC Genet. 2006; 6 Suppl 1:S61.
PMID: 16451674
PMC: 1866721.
DOI: 10.1186/1471-2156-6-S1-S61.
Maalej A, Rebai A, Ayadi A, Jouida J, Makni H, Ayadi H
J Genet. 2004; 83(1):65-71.
PMID: 15240910
DOI: 10.1007/BF02715830.
Arnheim N, Calabrese P, Nordborg M
Am J Hum Genet. 2003; 73(1):5-16.
PMID: 12772086
PMC: 1180590.
DOI: 10.1086/376419.
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.
Gurling H, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo B
Am J Hum Genet. 2001; 68(3):661-73.
PMID: 11179014
PMC: 1274479.
DOI: 10.1086/318788.
Two target regions of allelic loss on chromosome 9 in urinary-bladder cancer.
Ohgaki K, Minobe K, Kurose K, Iida A, Habuchi T, Ogawa O
Jpn J Cancer Res. 1999; 90(9):957-64.
PMID: 10551324
PMC: 5926161.
DOI: 10.1111/j.1349-7006.1999.tb00841.x.
High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.
Steingruber H, Dunham A, Coffey A, Clegg S, Howell G, Maslen G
Genome Res. 1999; 9(8):751-62.
PMID: 10447510
PMC: 310799.
Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
Boycott K, PEARCE W, Musarella M, Weleber R, Maybaum T, Birch D
Am J Hum Genet. 1998; 62(4):865-75.
PMID: 9529339
PMC: 1377021.
DOI: 10.1086/301781.
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
Mehenni H, Blouin J, Radhakrishna U, Bhardwaj S, Bhardwaj K, Dixit V
Am J Hum Genet. 1997; 61(6):1327-34.
PMID: 9399902
PMC: 1716075.
DOI: 10.1086/301644.
Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24.
Wang C, Ochoa B, Walker R, She J
Am J Hum Genet. 1997; 60(6):1461-7.
PMID: 9199567
PMC: 1716147.
DOI: 10.1086/515469.
Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.
Radhakrishna U, Blouin J, Mehenni H, Patel U, Patel M, Solanki J
Am J Hum Genet. 1997; 60(3):597-604.
PMID: 9042919
PMC: 1712530.
The structural basis of molecular genetic deletions. An integration of classical cytogenetic and molecular analyses in pancreatic adenocarcinoma.
Brat D, Hahn S, Griffin C, Yeo C, Kern S, Hruban R
Am J Pathol. 1997; 150(2):383-91.
PMID: 9033253
PMC: 1858276.
Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.
Weber B, Sander S, Kopp C, Walker D, Eckstein A, Wissinger B
Br J Ophthalmol. 1996; 80(8):745-9.
PMID: 8949721
PMC: 505593.
DOI: 10.1136/bjo.80.8.745.
Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region.
Datson N, Semina E, van Staalduinen A, Dauwerse H, Meershoek E, Heus J
Am J Hum Genet. 1996; 59(6):1297-305.
PMID: 8940275
PMC: 1914859.
Software for genetic linkage analysis: an update.
Bryant S
Mol Biotechnol. 1996; 5(1):49-61.
PMID: 8853016
DOI: 10.1007/BF02762412.
An integrated genetic map of Chromosome 6.
Cooke I, Cox S, Shelling A, Le Meuth V, Spurr N, Ganesan T
Mamm Genome. 1996; 7(2):157-9.
PMID: 8835537
DOI: 10.1007/s003359900040.
Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).
Gu X, Decorte R, Marynen P, Fryns J, Cassiman J, Raeymaekers P
J Med Genet. 1996; 33(1):52-5.
PMID: 8825049
PMC: 1051812.
DOI: 10.1136/jmg.33.1.52.
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
Bonne-Tamir B, DeStefano A, Briggs C, Adair R, Franklyn B, Weiss S
Am J Hum Genet. 1996; 58(6):1254-9.
PMID: 8651303
PMC: 1915077.
Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.
Xu S, Nakazawa M, Tamai M, Gal A
J Med Genet. 1995; 32(11):915-6.
PMID: 8592343
PMC: 1051751.
DOI: 10.1136/jmg.32.11.915.