| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00208975 |
| P698 | PubMed publication ID | 7705845 |
| P50 | author | Francis Collins | Q336658 |
| Val C. Sheffield | Q61268600 | ||
| P2093 | author name string | Y Shiloh | |
| Y Ziv | |||
| A Bar-Shira | |||
| A Sartiel | |||
| G Rotman | |||
| K Savitsky | |||
| S Gilad | |||
| L Vanagaite | |||
| C W Richard | |||
| J Weissenbach | |||
| M R James | |||
| V Uchenik | |||
| P2860 | cites work | Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. | Q34169664 |
| A radiation hybrid map of 506 STS markers spanning human chromosome 11. | Q34327393 | ||
| Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium | Q35204529 | ||
| Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23. | Q36768412 | ||
| Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis | Q37670654 | ||
| A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia. | Q41464927 | ||
| The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23 | Q46727645 | ||
| Physical and Genetic Mapping at the ATA/ATC Locus on Chromosome 11q22-23. | Q50222394 | ||
| A Haplotype Common to Intermediate Radiosensitivity Variants of Ataxia-telangiectasia in the UK. | Q50222430 | ||
| A haplotype common to intermediate radiosensitivity variants of ataxia-telangiectasia in the UK. | Q53769649 | ||
| A YAC Contig Spanning the Ataxia-Telangiectasia Locus (Groups A and C) at 11q22-q23 | Q57251206 | ||
| Three dinucleotide repeat polymorphisms at the ataxia-telangiectasia locus | Q72586815 | ||
| Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23 | Q72803037 | ||
| P433 | issue | 4 | |
| P921 | main subject | microsatellite | Q265193 |
| P304 | page(s) | 451-454 | |
| P577 | publication date | 1995-04-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | A high-density microsatellite map of the ataxia-telangiectasia locus | |
| P478 | volume | 95 |
| Q35881917 | A locus for Fanconi anemia on 16q determined by homozygosity mapping |
| Q24323579 | A single ataxia telangiectasia gene with a product similar to PI-3 kinase |
| Q33960818 | A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicity |
| Q45286458 | ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch population |
| Q45997989 | ATM haplotypes and associated mutations in Iranian patients with ataxia-telangiectasia: recurring homozygosity without a founder haplotype. |
| Q45107428 | ATM mutations on distinct SNP and STR haplotypes in ataxia-telangiectasia patients of differing ethnicities reveal ancestral founder effects |
| Q36671218 | ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer |
| Q61051652 | Allelic imbalance at chromosome region 11q23 in cervical carcinomas |
| Q41102995 | Ataxia-telangiectasia: a multifaceted genetic disorder associated with defective signal transduction |
| Q34384174 | Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations |
| Q80350472 | Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised alpha-fetoprotein |
| Q98178337 | Diabetes in Patients With Ataxia Telangiectasia: A National Cohort Study |
| Q74604746 | Frequent allelic imbalance at the ATM locus in DNA multiploid colorectal carcinomas |
| Q35681880 | Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia. |
| Q40952383 | Functional localization of a melanoma tumor suppressor gene to a small (< or = 2 Mb) region on 11q23. |
| Q44759219 | Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate |
| Q34142208 | Localization of multiple melanoma tumor-suppressor genes on chromosome 11 by use of homozygosity mapping-of-deletions analysis |
| Q42616265 | Nonclassical splicing mutations in the coding and noncoding regions of the ATM Gene: maximum entropy estimates of splice junction strengths |
| Q47770267 | Radiosensitivity and oxidative signalling in ataxia telangiectasia: an update |
| Q42950839 | The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1. |
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