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Publisher: Wiley-Blackwell

Volume 83, Number 4, 1 July 2019

The epigenetics of the hypothalamic‐pituitary‐adrenal axis in fetal development
pp. 195-213(19)
Authors: Montenegro, Yorran Hardman A.; Queiroga Nascimento, Denise; Assis, Thiago Oliveira; Santos‐Lopes, Simone Silva Dos

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Consanguinity: A blessing or menace at population level?
pp. 214-219(6)
Authors: Bhinder, Munir Ahmad; Sadia, Haleema; Mahmood, Nasir; Qasim, Muhammad; Hussain, Zawar; Rashid, Muhammad Mudassar; Zahoor, Muhammad Yasir; Bhatti, Rashid; Shehzad, Wasim; Waryah, Ali Muhammad; Jahan, Shah

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The mitochondrial DNA 4977‐bp deletion and copy number alteration in Han Chinese samples with uterine fibroids
pp. 220-230(11)
Authors: Luo, Yong; Zou, Yang; Wu, Juan; Zhang, Zi‐Yu; Liu, Fa‐Ying; Li, Li‐Ping; Huang, Ou‐Ping

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Regions of homozygosity as risk factors for multiple myeloma
pp. 231-238(8)
Authors: Went, Molly; Sud, Amit; Li, Ni; Johnson, David C.; Mitchell, Jonathan S.; Kaiser, Martin; Houlston, Richard S.

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Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4‐subunit SCN4B with atrial fibrillation
pp. 239-248(10)
Authors: Xiong, Hongbo; Yang, Qin; Zhang, Xiaoping; Wang, Pengxia; Chen, Feifei; Liu, Ying; Wang, Pengyun; Zhao, Yuanyuan; Li, Sisi; Huang, Yufeng; Chen, Shanshan; Wang, Xiaojing; Zhang, Hongfu; Yu, Dong; Tan, Chencheng; Fang, Cheng; Huang, Yuan; Wu, Gang; Wu, Yanxia; Cheng, Xiang; Liao, Yuhua; Zhang, Rongfeng; Yang, Yanzong; Ke, Tie; Ren, Xiang; Li, Hui; Tu, Xin; Xia, Yunlong; Xu, Chengqi; Chen, Qiuyun; Wang, Qing K.

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Influence of STAT4 gene polymorphisms in the pathogenesis of endometriosis
pp. 249-255(7)
Authors: Bianco, Bianca; Fernandes, Ramon Felix Martins; Trevisan, Camila Martins; Christofolini, Denise M.; Sanz‐Lomana, Carlos Millán; Bernabe, Javier Valero; Barbosa, Caio P.

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Two novel variants in the ATM gene causing ataxia‐telangiectasia, including a duplication of 90 kb: Utility of targeted next‐generation sequencing in detection of copy number variation
pp. 266-273(8)
Authors: Martin‐Rodriguez, Samuel; Calvo‐Ferrer, Alicia; Ortega‐Unanue, Nerea; Samaniego‐Jimenez, Laura; Sanz‐Izquierdo, Maria Pilar; Bernardo‐Gonzalez, Ivan

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Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations
pp. 278-284(7)
Authors: Gul, Hadia; Shah, Abdul Haleem; Harripaul, Ricardo; Mikhailov, Anna; Prajapati, Kamalben; Khan, Ejazullah; Ullah, Farman; Zubair, Muhammad; Ali, Muhammad Zeeshan; Shah, Ayesha Haleem; Salman, Said; Khan, Saadullah; Vincent, John B.; Khan, Muzammil Ahmad

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Association of rs10490924 in ARMS2/HTRA1 with age‐related macular degeneration in the Pakistani population
pp. 285-290(6)
Authors: Ayub, Humaira; Shafique, Sobia; Azam, Aisha; Muslim, Irfan; Qazi, Nauman A; Akhtar, Farah; Khan, Muhammad Asim; Ayub, Adil; Bashir, Shaheena; Bakker, Bjorn; Ahmed, Shakil; Azam, Maleeha; Hollander, Anneke I.; Qamar, Raheel

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