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Edisto Island Library

11 a.m. - 4 p.m.

Phone: (843) 869-2355

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9 a.m. – 8 p.m.

Phone: (843) 805-6888

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9 a.m. - 7 p.m.

Phone: (843) 766-6635

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9 a.m. - 6 p.m.

Phone: (843) 884-9741

St. Paul's/Hollywood Library

9 a.m. – 8 p.m.

Phone: (843) 889-3300

Otranto Road Library

9 a.m. – 8 p.m.

Phone: (843) 572-4094

Mt. Pleasant Library

9 a.m. – 8 p.m.

Phone: (843) 849-6161

McClellanville Library

9 a.m. – 6 p.m.

Phone: (843) 887-3699

Keith Summey North Charleston Library

9 a.m. – 8 p.m.

Phone: (843) 744-2489

Hurd/St. Andrews Library

9 a.m. – 8 p.m.

Phone: (843) 766-2546

Folly Beach Library

9 a.m. - 5:30 p.m.

Phone: (843) 588-2001

Dorchester Road Library

9 a.m. – 8 p.m.

Phone: (843) 552-6466

John L. Dart Library

9 a.m. – 7 p.m.

Phone: (843) 722-7550

Main Library

9 a.m. – 8 p.m.

Phone: (843) 805-6930

Bees Ferry West Ashley Library

9 a.m. – 8 p.m.

Phone: (843) 805-6892

John's Island Library

9 a.m. – 8 p.m.

Phone: (843) 559-1945

Baxter-Patrick James Island

9 a.m. – 8 p.m.

Phone: (843) 795-6679

Edgar Allan Poe/Sullivan's Island Library

Closed for renovations

Phone: (843) 883-3914

Mobile Library

9 a.m. - 5 p.m.

Phone: (843) 805-6909

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Academic Journal

Referral challenges for early-onset colorectal cancer: a qualitative study in UK primary care.

Authors : O'Neill, Orla M.; Coleman, Helen G.; Reid, Helen

Subjects: GENERAL practitioners; RESEARCH; DELAYED diagnosisNORTHERN Ireland; UNITED Kingdom

Source: BJGP Open; Dec2023, Vol. 7 Issue 4, p1-10, 10p

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Academic Journal

Prenatal and pre‐implantation genetic testing for monogenic disorders for germline cancer susceptibility gene variants: UK joint consensus guidance.

Authors : Wafik, Mohamed; Kilby, Mark David; Kulkarni, Anjana

Subjects: PRENATAL diagnosis; PRENATAL genetic testing; CANCER susceptibilityUNITED Kingdom

Source: BJOG: An International Journal of Obstetrics & Gynaecology; Dec2023, Vol. 130 Issue 13, p1563-1567, 5p

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Academic Journal

Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation.

Authors : de Jong, Vincent M. T.; Pruntel, Roelof; Steenbruggen, Tessa G.

Subjects: HEREDITARY cancer syndromes; CARCINOGENS; BRCA genesUNITED Kingdom

Source: Familial Cancer; Apr2023, Vol. 22 Issue 2, p151-154, 4p

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Academic Journal

Causal associations of thyroid function and dysfunction with overall, breast and thyroid cancer: A two‐sample Mendelian randomization study.

Authors : Yuan, Shuai; Kar, Siddhartha; Vithayathil, Mathew

Subjects: THYROID gland; THYROID cancer; BREAST cancerUNITED Kingdom

Source: International Journal of Cancer; Oct2020, Vol. 147 Issue 7, p1895-1903, 9p

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Academic Journal

Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort.

Authors : Mariathasan, Sashi; Andrews, Katrina A.; Thompson, Edward

Subjects: GENETIC testing; DISEASE risk factors; FIBROMASUNITED Kingdom

Source: Clinical Endocrinology; Oct2020, Vol. 93 Issue 4, p409-418, 10p

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Academic Journal

Cost-effectiveness analysis of reflex testing for Lynch syndrome in women with endometrial cancer in the UK setting.

Authors : Snowsill, Tristan M.; Ryan, Neil A. J.; Crosbie, Emma J.

Subjects: HEREDITARY nonpolyposis colorectal cancer; ENDOMETRIAL cancer; HEREDITARY cancer syndromesUNITED Kingdom

Source: PLoS ONE; 8/30/2019, Vol. 14 Issue 8, p1-18, 18p

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Academic Journal

Genetic predisposition to breast cancer: a surgical perspective.

Authors : Sakorafas, G. H.¹; Tsiotou, A. G.¹

Subjects: *BREAST cancer; *HEREDITARY cancer syndromesUNITED Kingdom

Source: British Journal of Surgery. Feb2000, Vol. 87 Issue 2, p149-162. 14p. 2 Charts.

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Academic Journal

Cost-effectiveness of pembrolizumab for previously treated MSI-H/dMMR solid tumours in the UK.

Authors : McCarthy G; MSD (UK) Ltd, London, UK.; Young K

Subjects: Antineoplastic Agents, Immunological* ; Colorectal Neoplasms*/Colorectal Neoplasms*/Colorectal Neoplasms*/drug therapy ; Brain Neoplasms* Turcot syndrome

Source: Journal of medical economics [J Med Econ] 2024 Jan-Dec; Vol. 27 (1), pp. 279-291. Date of Electronic Publication: 2024 Feb 19.Publisher: Taylor & Francis Country of Publication: England NLM ID: 9892255 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA(Communicated by Richard Cotton).

Authors : C.F. Taylor; R.S. Charlton; J. Burn

Subjects: GENETIC mutation; GENETIC disorders; GENESUNITED Kingdom

Source: Human Mutation; Dec2003, Vol. 22 Issue 6, p428-433, 6p

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Academic Journal

Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group.

Authors : Bakhuizen JJ; SIOPE Host Genome Working Group; CanGene-CanVar Clinical Guideline Working Group; Expert Network Members

Subjects: DEAD-box RNA Helicases*/DEAD-box RNA Helicases*/DEAD-box RNA Helicases*/genetics ; Neoplastic Syndromes, Hereditary*/Neoplastic Syndromes, Hereditary*/Neoplastic Syndromes, Hereditary*/diagnosis ; Neoplastic Syndromes, Hereditary*/Neoplastic Syndromes, Hereditary*/Neoplastic Syndromes, Hereditary*/genetics

Source: Familial cancer [Fam Cancer] 2021 Oct; Vol. 20 (4), pp. 337-348. Date of Electronic Publication: 2021 Jun 25.Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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