Search Results - "Burford DC"

Frequency of Chromosome Disorders In Patients with Sperm Number Anomaly.

Alternate Title: Sperm Sayısı Anomalisi Olan Hastalarda Kromozom Bozukluklarının Sıklığı.

Authors: Niyaz, Mehmet Abdullahı, Egzon Çelik, Zerrin Yılmaz

Source: Gazi Medical Journal. 2025, Vol. 36 Issue 1, p74-79. 6p.

HLA gene polymorphism is a modifier of age-related breast cancer penetrance in carriers of BRCA1 pathogenic alleles.

Authors: Kuligina ES Romanko AA Jankevic T et al.

Source: Breast cancer research and treatment [Breast Cancer Res Treat] 2025 Jan; Vol. 209 (2), pp. 341-354. Date of Electronic Publication: 2024 Sep 21.

Publication Type: Journal Article

Journal Info: Publisher: Kluwer Academic Country of Publication: Netherlands NLM ID: 8111104 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7217 (Electronic) Linking ISSN: 01676806 NLM ISO Abbreviation: Breast Cancer Res Treat Subsets: MEDLINE

Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays.

Authors: Fiegler H Gribble SM Burford DC et al.

Source: Journal of medical genetics [J Med Genet] 2003 Sep; Vol. 40 (9), pp. 664-70.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.

Authors: Shoichet, Sarah A. Waibel, Stefan Endruhn, Sonja et al.

Source: Amyotrophic Lateral Sclerosis. Jun2009, Vol. 10 Issue 3, p162-167. 6p. 3 Charts, 2 Graphs.

Origin of B chromosomes in Characidium alipioi (Characiformes, Crenuchidae) and its relationship with supernumerary chromosomes in other Characidium species.

Authors: Serrano, Érica Alves Utsunomia, Ricardo Scudeller, Patrícia Sobrinho et al.

Source: Comparative Cytogenetics. 2017, Vol. 11 Issue 1, p81-95. 15p.

KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.

Authors: Moreno-Igoa, María Hernández-Charro, Blanca Bengoa-Alonso, Amaya et al.

Source: BMC Medical Genetics. Aug2015, Vol. 16 Issue 1, p1-8. 8p.

Does greater patient involvement in healthcare decision-making affect malpractice complaints? A large case vignette survey.

Authors: Birkeland, Søren Bismark, Marie Barry, Michael J. et al.

Source: PLoS ONE. 7/2/2021, Vol. 16 Issue 7, p1-14. 14p.

Lessons from genetic profiling in soft tissue sarcomas.

Authors: Nilbert, M. Meza-Zepeda, L. A. Francis, P. et al.

Source: Acta Orthopaedica Scandinavica. Apr2004 Supplement 311, Vol. 75, p35-50.

Oligonucleotide Arrays vs. Metaphase-Comparative Genomic Hybridisation and BAC Arrays for Single-Cell Analysis: First Applications to Preimplantation Genetic Diagnosis for Robertsonian Translocation Carriers.

Authors: Ramos, Laia del Rey, Javier Daina, Gemma et al.

Source: PLoS ONE. Nov2014, Vol. 9 Issue 11, p1-15. 15p.

Use of DOP-PCR for amplification and labeling of BAC DNA for FISH.

Authors: Darouich, S Popovici, C Missirian, C et al.

Source: Biotechnic & Histochemistry. Feb2012, Vol. 87 Issue 2, p117-121. 5p.

The importance of a genetic component in longitudinal birth cohorts.

Authors: Golding, Jean¹ jean.golding@bristol.ac.uk

Source: Paediatric & Perinatal Epidemiology. Jul2009 Supplement 1, Vol. 23, p174-184. 11p. 1 Diagram, 1 Chart.

Men's view on participation in decisions about prostate-specific antigen (PSA) screening: patient and public involvement in development of a survey.

Authors: Birkeland, Søren Pedersen, Susanne S. Haakonsson, Anders K. et al.

Source: BMC Medical Informatics & Decision Making. 4/6/2020, Vol. 20 Issue 1, p1-10. 10p. 7 Charts.

Interstitial Deletion 4q due to a Complex Rearrangement Involving Chromosomes 1, 2, 4, 8, 14 and 16.

Alternate Title: Kromozom 1, 2, 4, 8, 14 ve 16'yı Içeren Kompleks Kromozom Anomalisinin Yol Açtığı Inserstisyal 4q Delesyonu.

Authors: Toksoy, Güven Röthlisberger, Benno Turkover, Bilge et al.

Source: Gazi Medical Journal. 2018, Vol. 29 Issue 3, p256-260. 5p.

Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing.

Authors: Aristidou, Constantia Koufaris, Costas Theodosiou, Athina et al.

Source: PLoS ONE. 1/10/2017, Vol. 12 Issue 1, p1-18. 18p.

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Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.

Authors: Tabet, Anne-Claude Verloes, Alain Pilorge, Marion et al.

Source: Molecular Autism. 2015, Vol. 6 Issue 1, p1-14. 14p.

Balanced complex chromosome rearrangement in male infertility: case report and literature review.

Authors: Nguyen, M. H. Morel, F. Pennamen, P. et al.

Source: Andrologia. Mar2015, Vol. 47 Issue 2, p178-185. 8p.

Single Origin of Sex Chromosomes and Multiple Origins of B Chromosomes in Fish Genus Characidium.

Authors: Pansonato-Alves, José Carlos Serrano, Érica Alves Utsunomia, Ricardo et al.

Source: PLoS ONE. Sep2014, Vol. 9 Issue 9, p1-10. 10p.

Interaction-based evolution: how natural selection and nonrandom mutation work together.

Authors: Livnat, Adi¹ adi@vt.edu

Source: Biology Direct. 10/18/2013, Vol. 8 Issue 1, p1-53. 53p. 3 Diagrams.

Are morphological criteria sufficient for the identification of circulating tumor cells in renal cancer?

Authors: El-Heliebi, Amin Kroneis, Thomas Zöhrer, Evelyn et al.

Source: Journal of Translational Medicine. 2013, Vol. 11 Issue 1, p1-17. 17p.