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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Disease and TCAP[original query]
HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer.
British journal of cancer 2006 Dec 95 (12): 1689-95.
Benusiglio P R, Pharoah P D, Smith P L, Lesueur F, Conroy D, Luben R N, Dew G, Jordan C, Dunning A, Easton D F, Ponder B A
Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.
Human mutation 2009 Mar 30 (3): 363-70.
Andersen Paal Skytt, Havndrup Ole, Hougs Lotte, Sørensen Karina M, Jensen Morten, Larsen Lars Allan, Hedley Paula, Thomsen Alex Rojas Bie, Moolman-Smook Johanna, Christiansen Michael, Bundgaard Henni
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
Clinical and translational science 2008 May 1 (1): 21-6.
Hershberger Ray E, Parks Sharie B, Kushner Jessica D, Li Duanxiang, Ludwigsen Susan, Jakobs Petra, Nauman Deirdre, Burgess Donna, Partain Julie, Litt Micha
Detection of Variants in Patients with Idiopathic Ventricular Fibrillation by Whole-exome Sequencing.
Annals of clinical and laboratory science 2018 8 48 (4): 427-434.
Chang Ya-Sian, Lee Chien-Chin, Huang Hsi-Yuan, Lin Kuo-Hung, Chen Jan-Yow, Chang Kuan-Cheng, Chang Jan-Gow
Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy.
Orphanet journal of rare diseases 2020 6 15 (1): 160.
Liang Wen-Chen, Jong Yuh-Jyh, Wang Chien-Hua, Wang Chen-Hua, Tian Xia, Chen Wan-Zi, Kan Tzu-Min, Minami Narihiro, Nishino Ichizo, Wong Lee-Jun
Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy.
Revista portuguesa de cardiologia 2020 6 39 (6): 317-327.
Toste Alexandra, Perrot Andreas, Özcelik Cemil, Cardim Nu
TCAP gene is not a common cause of cardiomyopathy in Iranian patients.
European journal of medical research 2023 9 28 (1): 376.
Zahra Alaei, Nasrin Zamani, Bahareh Rabbani, Nejat Mahdi
Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.
Orphanet journal of rare diseases 2023 11 18 (1): 356.
Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-Ze Zheng, Liang-Liang Qiu, Zhi-Xian Ye, Hai-Zhu Chen, Min-Ting Lin, Ning Wang, Zhi-Qiang Wa
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