| scholarly article | Q13442814 |
| case report | Q2782326 |
| P2093 | author name string | Green J | |
| Ko E | |||
| Martin RH | |||
| Barclay L | |||
| Rademaker AW | |||
| P2860 | cites work | Mutation of a mutL homolog in hereditary colon cancer | Q28114939 |
| hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds | Q28246692 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Sex and the single cell: meiosis in yeast | Q33775500 | ||
| Double or nothing: a Drosophila mutation affecting meiotic chromosome segregation in both females and males. | Q33962684 | ||
| XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region | Q35197098 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
| Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions | Q67265730 | ||
| MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
| Prevalence of chromosome abnormalities during human gestation and implications for studies of environmental mutagens | Q72482716 | ||
| Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm | Q73422107 | ||
| A human compound heterozygote for two MLH1 missense mutations | Q73777232 | ||
| Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human spermatozoa using multicolour fluorescence in-situ hybridization | Q77525163 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Lynch syndrome | Q783644 |
| colon cancer | Q18555025 | ||
| P304 | page(s) | 1149-1152 | |
| P577 | publication date | 2000-03-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Analysis of aneuploidy frequencies in sperm from patients with hereditary nonpolyposis colon cancer and an hMSH2 mutation | |
| P478 | volume | 66 |
| Q26770311 | 1(st) trimester miscarriage: four decades of study |
| Q47445150 | Analysis of factors decreasing testis weight in MRL mice |
| Q35587019 | Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes |
| Q37050787 | Do heat stress and deficits in DNA repair pathways have a negative impact on male fertility? |
| Q34615262 | Frequent germline mutations and somatic repeat instability in DNA mismatch-repair-deficient Caenorhabditis elegans |
| Q34164887 | Mitochondrial genome instability in human cancers |
| Q40727010 | Mosaic AZF deletions and susceptibility to testicular tumors |
| Q80216021 | Sperm chromosome aneuploidy as related to male factor infertility and some ultrastructure defects |
| Q34044815 | The origin of abnormalities in recurrent aneuploidy/polyploidy |
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