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Current Opinion in Oncology, ISSN 1040-8746, 03/2019, Volume 31, Issue 2, pp. 108 - 113
PURPOSE OF REVIEWGenetic mosaicism is the presence of a somatic mutation in a subset of cells that differs from the inherited germline genome. Detectable... 
clonal hematopoiesis | genetic mosaicism | RISK | CHROMOSOME Y | SOMATIC MOSAICISM | HEMATOPOIESIS | ONCOLOGY | DISEASE | cancer risk | aging | MUTATIONS | DETECTABLE CLONAL MOSAICISM | DELETIONS | chromosomal alterations | AGE
Journal Article
Science, ISSN 0036-8075, 10/2010, Volume 330, Issue 6000, pp. 46 - 47
Somatic revertant mosaicism-the coexistence of cells carrying inherited genetic mutations with cells that have undergone spontaneous changes that correct the... 
T lymphocytes | Keratins | Epidermal cells | Genes | Stem cells | PERSPECTIVES | Mosaicism | Skin | Genetic mutation | Hematopoietic stem cells | Ichthyosis | 2ND-SITE MUTATIONS | REVERTANT MOSAICISM | MULTIDISCIPLINARY SCIENCES | WISKOTT-ALDRICH-SYNDROME | SIBLINGS | PATIENT | EPIDERMOLYSIS-BULLOSA | SOMATIC MOSAICISM | LYMPHOCYTES | Mutations | Genetics | Patients | Spontaneous | Bearing
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 02/2019, Volume 56, Issue 2, pp. 81 - 88
Background Mutations in the PCDH19 gene have mainly been reported in female patients with epilepsy. To date, PCDH19 mutations have been reported in hundreds of... 
epilepsy | mddpcr | mosaicism | pcdh19 | sequencing | INFANTILE EPILEPTIC ENCEPHALOPATHY | MENTAL-RETARDATION | GENE | PARENTAL MOSAICISM | GENETICS & HEREDITY | FEMALES | SPECTRUM | SOMATIC MOSAICISM | Convulsions & seizures | Phenotypes | Next-generation sequencing | Epilepsy | Families & family life | Mosaicism | Mutation | Genetic counselling | Deoxyribonucleic acid--DNA | Genotypes | Somatic Mosaicism | 1506
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 8, pp. 969 - 978
Journal Article
JAMA Neurology, ISSN 2168-6149, 07/2016, Volume 73, Issue 7, pp. 836 - 845
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 05/2018, Volume 28, Issue 5, pp. 422 - 426
Myopathies due to mutations in the skeletal muscle ryanodine receptor gene are amongst the most common non-dystrophic neuromuscular disorders and have been... 
Central Core Disease (CCD) | Mosaicism | Skeletal muscle ryanodine receptor (RYR1) gene | GERMLINE MOSAICISM | MALIGNANT HYPERTHERMIA | 1 GENE | SOMATIC MOSAICISM | NEUROSCIENCES | CLINICAL NEUROLOGY | FAMILY | HETEROGENEITY | RYR1 GENE | MUTATIONS | LINKED MYOTUBULAR MYOPATHY | COMMON-CAUSE | Parenting | Muscles | Neurosciences | Children's hospitals | Genetic screening | Medical genetics
Journal Article
by Machiela, Mitchell J and Zhou, Weiyin and Zhou, Baosen and Sampson, Joshua N and Dean, Michael C and Jacobs, Kevin B and Black, Amanda and Brinton, Louise A and Chang, I-Shou and Chen, Constance and Chen, Chu and Chen, Kexin and Cook, Linda S and Cook, Michael B and Crous Bou, Marta and De Vivo, Immaculata and Doherty, Jennifer and Friedenreich, Christine M and Gaudet, Mia M and Haiman, Christopher A and Hankinson, Susan E and Hartge, Patricia and Henderson, Brian E and Hong, Yun-Chul and Hosgood, H. Dean and Hsiung, Chao A and Hu, Wei and Hu, Nan and Hunter, David J and Jessop, Lea and Kim, Hee Nam and Kim, Young Tae and Kim, Yeul Hong and Klein, Robert and Kraft, Peter and Lan, Qing and Lin, Dongxin and Liu, Jianjun and Le Marchand, Loic and Liang, Xiaolin and Lissowska, Jolanta and Lu, Lingeng and Magliocco, Anthony M and Matsuo, Keitaro and Olson, Sara H and Orlow, Irene and Park, Jae Yong and Pooler, Loreall and Prescott, Jennifer and Rastogi, Radhai and Risch, Harvey A and Schumacher, Fredrick and Seow, Adeline and Setiawan, Veronica Wendy and Shen, Hongbing and Sheng, Xin and Shin, Min-Ho and Shu, Xiao-Ou and VanDen Berg, David and Wang, Zhaoming and Wang, Jiu-Cun and Wentzensen, Nicolas and Wong, Maria Pik and Wu, Tangchun and Wu, Xifeng and Wu, Chen and Wu, Yi-Long and Xia, Lucy and Yang, Hannah P and Yang, Pan-Chyr and Zheng, Wei and Abnet, Christian C and Albanes, Demetrius and Aldrich, Melinda C and Amos, Christopher and Amundadottir, Laufey T and Berndt, Sonja I and Blot, William J and Bock, Cathryn H and Bracci, Paige M and Burdett, Laurie and Buring, Julie E and Butler, Mary A and Carreón, Tania and Chatterjee, Nilanjan and Chung, Charles C and Cullen, Michael and Davis, Faith G and Ding, Ti and Duell, Eric J and Epstein, Caroline G and Fan, Jin-Hu and Figueroa, Jonine D and Fraumeni, Joseph F and Freedman, Neal D and Fuchs, Charles S and Gao, Yu-Tang and Gapstur, Susan M and Patiño-Garcia, Ana and Garcia-Closas, Montserrat and ... and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Näringsforskning and Onkologi
The American Journal of Human Genetics, ISSN 0002-9297, 03/2015, Volume 96, Issue 3, pp. 487 - 497
Journal Article
Human Mutation, ISSN 1059-7794, 09/2008, Volume 29, Issue 9, pp. 1118 - 1124
Journal Article