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by Li, XF and Liu, Y and Yue, S and Wang, L and Zhang, TJ and Guo, CX and Hu, WJ and Kagan, KO and Wu, QQ
MEDICINE, ISSN 0025-7974, 11/2017, Volume 96, Issue 45, pp. e8474 - e8474
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 06/2019, Volume 66, Issue 6, pp. e27715 - n/a
Mosaic genome‐wide paternal uniparental disomy is an infrequently described disorder in which affected individuals have signs and symptoms that may resemble... 
tumors | paternal uniparental disomy | syndrome | body asymmetry | ISODISOMY | ONCOLOGY | PEDIATRICS | HEMATOLOGY | BECKWITH-WIEDEMANN SYNDROME | FEATURES | Genomics | Tumors
Journal Article
Journal Article
Epigenetics, ISSN 1559-2294, 10/2012, Volume 7, Issue 10, pp. 1142 - 1150
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2012, Volume 109, Issue 25, pp. 9947 - 9952
Journal Article
Genes, Chromosomes and Cancer, ISSN 1045-2257, 01/2018, Volume 57, Issue 1, pp. 42 - 47
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 04/2014, Volume 56, Issue 4, pp. 386 - 389
Infantile neuroaxonal dystrophy ( INAD ) is a rare autosomal recessive neurodegenerative disorder caused by mutations in the phospholipase A2 group 6 ( Pla2G6... 
NEURODEGENERATION | DISORDERS | PEDIATRICS | SPECTRUM | PLA2G6 | CHILDHOOD | CLINICAL NEUROLOGY | BRAIN IRON | Magnetic Resonance Imaging | Uniparental Disomy - genetics | Group VI Phospholipases A2 - genetics | Humans | Female | Infant | Uniparental Disomy - physiopathology | Neuroaxonal Dystrophies - genetics | Index Medicus
Journal Article