Menu

West Ashley Library

Closed

Phone: (843) 766-6635

Wando Mount Pleasant Library

Closed

Phone: (843) 805-6888

Village Library

Closed

Phone: (843) 884-9741

St. Paul's/Hollywood Library

Closed

Phone: (843) 889-3300

Otranto Road Library

Closed

Phone: (843) 572-4094

Mt. Pleasant Library

Closed

Phone: (843) 849-6161

McClellanville Library

Closed

Phone: (843) 887-3699

Keith Summey North Charleston Library

Closed

Phone: (843) 744-2489

John's Island Library

Closed

Phone: (843) 559-1945

Hurd/St. Andrews Library

Closed

Phone: (843) 766-2546

Folly Beach Library

Closed

Phone: (843) 588-2001

Miss Jane's Building (Edisto Library Temporary Location)

Closed

Phone: (843) 869-2355

Dorchester Road Library

Closed

Phone: (843) 552-6466

John L. Dart Library

Closed

Phone: (843) 722-7550

Baxter-Patrick James Island

Closed

Phone: (843) 795-6679

Main Library

2 p.m. – 5 p.m.

Phone: (843) 805-6930

Bees Ferry West Ashley Library

Closed

Phone: (843) 805-6892

Edgar Allan Poe/Sullivan's Island Library

Closed for renovations

Phone: (843) 883-3914

Mobile Library

Closed

Phone: (843) 805-6909

Item request has been placed!

Item request cannot be made.

Processing Request

Search Results

Display Settings

Results per page: 10

Sort By: Relevance

Your Filters

Subject : ankle Subject : electric stimulation Subject : exercise Subject : genetic mutation Subject : glycogen storage disease type ii Subject : health surveys Subject : medical history taking Subject : quality of life Filter by : Subject

Item request has been placed!

Item request cannot be made.

Processing Request

Academic Journal

Brief Report: Evidence of Autism Spectrum Disorder Caused by a Mutation in ATRX Gene: A Case Report.

Authors : López-Garrido, María-Pilar; Carrascosa-Romero, María-Carmen; Montero-Hernández, Minerva

Subjects: DIAGNOSIS of autism; BRAIN; GENETIC mutationSPAIN

Source: Journal of Autism & Developmental Disorders. Jan2024, Vol. 54 Issue 1, p379-388. 10p.

Read Online Read More Add to Saved list

Academic Journal

Exploring the diversity of CFTR gene mutations in cystic fibrosis individuals of South Asia.

Authors : Rafique, Hassan (AUTHOR); Safdar, Anum (AUTHOR); Ghani, Muhammad Usman (AUTHOR)

Subjects: CYSTIC fibrosis transmembrane conductance regulator; CYSTIC fibrosis; GENETIC mutationSOUTH Asia

Source: Journal of Asthma. Jun2024, Vol. 61 Issue 6, p511-519. 9p.

Read More Add to Saved list

Academic Journal

A chorea-acanthocytosis patient with novel mutations in the VPS13A gene without acanthocyte.

Authors : Jin, Shan (AUTHOR); Sun, Zhengzhe (AUTHOR); Fang, Xiang (AUTHOR)

Subjects: MOVEMENT disorders; GENETIC testing; GENETIC mutation

Source: Neurological Sciences. May2024, Vol. 45 Issue 5, p2057-2061. 5p.

Read More Add to Saved list

Academic Journal

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center.

Authors : Du, Xiaoli; Glass, Jennifer Elaine; Balow, Stephanie

Subjects: DIAGNOSIS of fragile X syndrome; DIAGNOSIS of autism; GENETIC mutationOHIO

Source: Journal of Autism & Developmental Disorders. Nov2022, Vol. 52 Issue 11, p4828-4842. 15p. 3 Diagrams, 2 Charts, 2 Graphs.

Read Online Read More Add to Saved list

Academic Journal

Evaluation of the value of genetic testing for cystinuria in the Danish population of English bulldogs.

Authors : Fitzwilliams, Therese¹ (AUTHOR); Wolff‐Sneedorff, Julie L.² (AUTHOR); Fredholm, Merete² (AUTHOR)

Subjects: *BULLDOG; *GENETIC testing; *MISSENSE mutation

Source: Animal Genetics. Aug2023, Vol. 54 Issue 4, p566-569. 4p.

Read Online Read More Add to Saved list

Academic Journal

Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss.

Authors : Jin, ZhanGuo (AUTHOR); Zhu, Qingwen (AUTHOR); Lu, Yu (AUTHOR)

Subjects: GENETIC mutation; SEQUENCE analysis; GENETIC testingCHINA

Source: Acta Oto-Laryngologica. May2022, Vol. 142 Issue 5, p448-453. 6p.

Read Online Read More Add to Saved list

Academic Journal

Case Report: Association of Comorbid Psychiatric Disorders and Sigmoid Prolapse with de novo POGZ Mutation.

Authors : Wright, Cary M.; Guter, Stephen J.; Cook, Edwin H.

Subjects: DIAGNOSIS of obsessive-compulsive disorder; DIAGNOSIS of bipolar disorder; DIAGNOSIS of autism

Source: Journal of Autism & Developmental Disorders. Mar2022, Vol. 52 Issue 3, p1408-1411. 4p. 1 Chart.

Read Online Read More Add to Saved list

Academic Journal

Diagnostic workup of rhabdomyolysis: Genetic testing should precede neurophysiological testing.

Authors : Voermans, Nicol C.¹ (AUTHOR) ; Bhai, Salman^2,3 (AUTHOR); Laforet, Pascal⁴ (AUTHOR)

Subjects: *GENETIC testing; *RHABDOMYOLYSIS; *LSD (Drug)

Source: Muscle & Nerve. Jul2024, p1. 4p. 2 Illustrations.

Read More Add to Saved list

Academic Journal

Trichoscopic findings in neonatal alopecia in oro‐facial‐digital syndrome type 1.

Authors : Martinez‐Molina, Manel¹ (AUTHOR); Carmona‐Rocha, Elena¹ (AUTHOR); Gil‐Lianes, Javier¹ (AUTHOR)

Subjects: *BALDNESS; *GENETIC testing; *CUTANEOUS manifestations of general diseases

Source: Pediatric Dermatology. Jul2024, p1. 4p. 2 Illustrations.

Read More Add to Saved list

Academic Journal

Atypical Droplet Digital Polymerase Chain Reaction Patterns That Indicate Uncommon but Clinically Actionable EGFR Mutations in Lung Cancer.

Authors : Lechner, Adam; Rai, Anooja; Rojas-Rudilla, Vanesa

Subjects: DIGITAL technology; BINDING sites; POLYMERASE chain reaction

Source: Archives of Pathology & Laboratory Medicine. May2024, Vol. 148 Issue 5, p553-558. 6p.

Read Online Read More Add to Saved list