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French Protestant Refugees.
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- Notes & Queries, 1856, v. 1, n. 11, p. 222-c
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- Article
Parish Clerks' Company.
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- Notes & Queries, 1853, v. 8, n. 210, p. 452-g
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- Article
The Saltpetre Man.
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- Notes & Queries, 1853, v. 8, n. 208, p. 399
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- Article
BOOKS BURNED BY THE COMMON HANGMAN.
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- Notes & Queries, 1853, v. 8, n. 206, p. 348-a
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- Article
“De la Schola de Sclavoni.”.
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- Notes & Queries, 1853, v. 8, n. 206, p. 339-c
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- Article
Huguenots in Ireland.
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- Notes & Queries, 1852, v. 6, n. 157, p. 423-a
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- Article
Primary Intracerebral Haemorrhage in the Oxfordshire Community Stroke Project.
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- Cerebrovascular Diseases, 1995, v. 5, n. 1, p. 26, doi. 10.1159/000107814
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- Article
Primary Intracerebral Haemorrhage in the Oxfordshire Community Stroke Project.
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- Cerebrovascular Diseases, 1993, v. 3, n. 6, p. 343, doi. 10.1159/000108729
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- Publication type:
- Article
Targeting Tropomyosin Receptor Kinase in Cutaneous CYLD Defective Tumors With Pegcantratinib: The TRAC Randomized Clinical Trial.
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- 2018
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- Publication type:
- journal article
An investigation of folate-related genetic factors in the determination of birthweight.
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- Paediatric & Perinatal Epidemiology, 2005, v. 19, n. 5, p. 360, doi. 10.1111/j.1365-3016.2005.00662.x
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- Publication type:
- Article
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes.
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- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00279-3
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- Publication type:
- Article
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
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- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00241-1
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- Publication type:
- Article
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0127-3
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- Publication type:
- Article
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0106-8
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- Publication type:
- Article
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.
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- Hereditary Cancer in Clinical Practice, 2017, p. 1, doi. 10.1186/s13053-017-0078-5
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- Publication type:
- Article
Frederick Field, M.A., LL.D.
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- Expository Times, 1897, v. 8, n. 7, p. 325, doi. 10.1177/001452469700800711
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- Publication type:
- Article
Frederick Field, M.A., EE.D.
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- Expository Times, 1897, v. 8, n. 6, p. 274, doi. 10.1177/001452469700800609
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- Publication type:
- Article
Frederick Field, M.A., LL.D.
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- Expository Times, 1897, v. 8, n. 4, p. 160, doi. 10.1177/001452469700800405
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- Publication type:
- Article
EASI—enrichment of alternatively spliced isoforms.
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- Nucleic Acids Research, 2006, v. 34, n. 15, p. e103, doi. 10.1093/nar/gkl592
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- Publication type:
- Article
‘Malignant’ congenital cardiovascular disease in twins with William's syndrome.
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- Cardiology in the Young, 1993, v. 3, n. 4, p. 435, doi. 10.1017/S104795110000189X
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- Publication type:
- Article
Three decades of the Human Genome Organization.
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 11, p. 3314, doi. 10.1002/ajmg.a.62512
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- Publication type:
- Article
Transition from cylindroma to spiradenoma in CYLD-defective tumours is associated with reduced DKK2 expression.
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- Journal of Pathology, 2011, v. 224, n. 3, p. 309, doi. 10.1002/path.2896
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- Publication type:
- Article
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.
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- Nature Genetics, 2007, v. 39, n. 8, p. 963, doi. 10.1038/ng2083
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- Publication type:
- Article
Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human.
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- Nature Genetics, 2003, v. 34, n. 4, p. 403, doi. 10.1038/ng1220
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- Publication type:
- Article
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.
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- Nature Genetics, 2001, v. 28, n. 4, p. 350, doi. 10.1038/ng571
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- Article
A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability.
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- Nature Genetics, 2000, v. 26, n. 3, p. 362, doi. 10.1038/81691
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- Article
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.
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- Nature Genetics, 2000, v. 25, n. 1, p. 42, doi. 10.1038/75578
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- Article
Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnancies.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 706, doi. 10.1002/(SICI)1097-0223(199908)19:8<706::AID-PD613>3.0.CO;2-W
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- Publication type:
- Article
Lynch Syndrome: History, Causes, Diagnosis, Treatment and Prevention (CAPP2 Trial).
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- Digestive Diseases, 2012, v. 30, p. 39, doi. 10.1159/000341892
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- Publication type:
- Article
'The next lady has a heart defect'.
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- BJOG: An International Journal of Obstetrics & Gynaecology, 1987, v. 94, n. 2, p. 97, doi. 10.1111/j.1471-0528.1987.tb02332.x
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- Publication type:
- Article
Employment and advice regarding careers for adults with congenital heart disease.
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- Cardiology in the Young, 2005, v. 15, n. 4, p. 391, doi. 10.1017/S104795110500082X
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- Publication type:
- Article
Genetic Variation in VEGF Does Not Contribute Significantly to the Risk of Congenital Cardiovascular Malformation.
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- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004978
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- Article
Mutation (variation) databases and registries: a rationale for coordination of efforts.
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- 2011
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- Publication type:
- Letter
A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.
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- Human Genetics, 2004, v. 115, n. 2, p. 139, doi. 10.1007/s00439-004-1134-6
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- Publication type:
- Article
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2 : A Prospective Lynch Syndrome Database Study.
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- Journal of Clinical Medicine, 2021, v. 10, n. 13, p. 2856, doi. 10.3390/jcm10132856
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- Article
O09 Microsatellite-unstable sporadic sebaceous and duodenal tumours are associated with loss of mismatch protein expression.
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- British Journal of Dermatology, 2024, v. 190, n. 6, p. e72, doi. 10.1093/bjd/ljae105.009
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- Article
Response to 'Cutaneous squamous cell carcinoma is associated with Lynch syndrome: widening the spectrum of Lynch syndrome‐associated tumours'.
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- British Journal of Dermatology, 2022, v. 186, n. 5, p. 913, doi. 10.1111/bjd.20970
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- Article
Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay.
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- Cancers, 2022, v. 14, n. 15, p. 3838, doi. 10.3390/cancers14153838
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- Article
How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future Strategies.
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- Cancers, 2021, v. 13, n. 3, p. 406, doi. 10.3390/cancers13030406
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- Article
Mild cognitive impairment in Parkinson's disease.
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- Age & Ageing, 2013, v. 42, n. 5, p. 567, doi. 10.1093/ageing/aft085
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- Article
Amantadine-induced myoclonus in a patient with progressive supranuclear palsy.
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- Age & Ageing, 2012, v. 41, n. 5, p. 695, doi. 10.1093/ageing/afs043
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- Publication type:
- Article
Twenty-year trends in prevalence and survival of Down syndrome.
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- European Journal of Human Genetics, 2008, v. 16, n. 11, p. 1336, doi. 10.1038/ejhg.2008.122
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- Article
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 516, doi. 10.1038/sj.ejhg.5200846
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- Publication type:
- Article
Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach.
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- European Journal of Human Genetics, 2000, v. 8, n. 1, p. 49, doi. 10.1038/sj.ejhg.5200393
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- Publication type:
- Article
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.
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- NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00603-z
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- Publication type:
- Article
Risk-stratified faecal immunochemical testing (FIT) for urgent colonoscopy in Lynch syndrome during the COVID-19 pandemic.
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- BJS Open, 2023, v. 7, n. 5, p. 1, doi. 10.1093/bjsopen/zrad079
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- Article
MLH1 Differential Allelic Expression in Mutation Carriers and Controls.
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- Annals of Human Genetics, 2010, v. 74, n. 6, p. 479, doi. 10.1111/j.1469-1809.2010.00603.x
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- Publication type:
- Article
Aspirin: 120 years of innovation. A report from the 2017 Scientific Conference of the International Aspirin Foundation, 14 September 2017, Charité, Berlin.
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- Ecancermedicalscience, 2018, v. 12, n. 792-818, p. 1, doi. 10.3332/ecancer.2018.813
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- Article
Harveian Oration 2019: Prediction and prevention in the genomic era.
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- Clinical Medicine, 2020, v. 20, n. 1, p. 8, doi. 10.7861/clinmed.ed.20.1.harv
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- Publication type:
- Article
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation.
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- Brain: A Journal of Neurology, 2009, v. 132, n. 6, p. e109, doi. 10.1093/brain/awn274
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- Publication type:
- Article