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Publisher: Wiley-Blackwell

Volume 83, Number 2, 1 March 2019

DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy
pp. 73-81(9)
Authors: Maretina, Marianna; Egorova, Anna; Baranov, Vladislav; Kiselev, Anton

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Genetic variations and population data on five supplementary STR markers in Lebanon
pp. 82-85(4)
Authors: El Andari, Ansar; Mourad, Lama; Mansour, Issam

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Expression patterns common and unique to ulcerative colitis and celiac disease
pp. 86-94(9)
Authors: Medrano, Luz María; Pascual, Virginia; Bodas, Andrés; López‐Palacios, Natalia; Salazar, Isabel; Espino‐Paisán, Laura; González‐Pérez, Beatriz; Urcelay, Elena; Mendoza, Juan Luis; Núñez, Concepción

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A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole‐exome sequencing in a Chinese family with dilated cardiomyopathy
pp. 95-99(5)
Authors: Zhang, Shu‐Bing; Liu, Yu‐Xing; Fan, Liang‐Liang; Huang, Hao; Li, Jing‐Jing; Jin, Jie‐Yuan; Xiang, Rong

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Confirmation of BRD4 haploinsufficiency role in Cornelia de Lange–like phenotype and delineation of a 19p13.12p13.11 gene contiguous syndrome
pp. 100-109(10)
Authors: Alesi, Viola; Dentici, Maria Lisa; Loddo, Sara; Genovese, Silvia; Orlando, Valeria; Calacci, Chiara; Pompili, Daniele; Dallapiccola, Bruno; Digilio, Maria Cristina; Novelli, Antonio

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IL8 and IL17A polymorphisms associated with multibacillary leprosy and reaction type 1 in a mixed population from southern Brazil
pp. 110-114(5)
Authors: Aquino, Julimary Suematsu; Ambrosio‐Albuquerque, Eliane Papa; Alves, Hugo Vicentin; Macedo, Luciana Conci; Visentainer, Lorena; Sell, Ana Maria; Visentainer, Jeane Eliete Laguila

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