[Genotype and phenotype correlation of phenylalanine hydroxylase deficiency among patients from Henan]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 300-5.

Public Health Genomics Knowledge Base (v1.2)

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• [Genotype and phenotype correlation of phenylalanine hydroxylase deficiency among patients from Henan].
  Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 300-5.
  Zhao Dehua, Li Xiaole, Jia Chenlu, Ni Min, Kong Xiangdo
• Genetic background of hyperphenylalaninemia in Nagasaki, Japan.
  Pediatrics international : official journal of the Japan Pediatric Society 2016 May 58 (5): 431-3.
  Dateki Sumito, Watanabe Satoshi, Nakatomi Akiko, Kinoshita Eiichi, Matsumoto Tadashi, Yoshiura Koh-Ichiro, Moriuchi Hiroyu
• Molecular epidemiology, genotype-phenotype correlation and BH4 responsiveness in Spanish patients with phenylketonuria.
  Journal of human genetics 2016 Apr .
  Aldámiz-Echevarría Luis, Llarena Marta, Bueno María A, Dalmau Jaime, Vitoria Isidro, Fernández-Marmiesse Ana, Andrade Fernando, Blasco Javier, Alcalde Carlos, Gil David, García María C, González-Lamuño Domingo, Ruiz Mónica, Ruiz María A, Peña-Quintana Luis, González David, Sánchez-Valverde Felix, Desviat Lourdes R, Pérez Belen, Couce María
• A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height.
  Journal of medical genetics 2016 Feb .
  North Teri-Louise, Ben-Shlomo Yoav, Cooper Cyrus, Deary Ian J, Gallacher John, Kivimaki Mika, Kumari Meena, Martin Richard M, Pattie Alison, Sayer Avan Aihie, Starr John M, Wong Andrew, Kuh Diana, Rodriguez Santiago, Day Ian N
• Successful Linkage Analysis in Classical Phenylketonuria Families Followed by Direct Sequencing and Mutation Detection.
  Clinical laboratory 2016 62 (3): 311-6.
  Silawi Mohammad, Haqparast Somayyeh, Tabei Seyed Mohammad Bagh

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