decay
- 期刊名称Physical Review C
- 作者Bahcall, John N.; Lisi, E.; Alburger, D. E.; De Braeckeleer, L.; Freedman, S. J.; Napolitano, J.
- 卷第54卷
- 期第1期
- 印刷ISSN0556-2813
- 电子ISSN1089-490X
- 文件大小242.43KB
- 发表时间1996-7-1
- DOI10.1103/PhysRevC.54.411
- 页码411-422
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyHong, Y. · Human Molecular Genetics · 1996
Prenatal cytogenomic identification and molecular refinement of compound heterozygous <i>STRC</i> deletion breakpointsShi, Lisong; Bai, Yan; Kharbutli, Yara; Oza, Andrea M.; Amr, Sami S.; Edelmann, Lisa; Mehta, Lakshmi; Scott, Stuart A. · Molecular Genetics & Genomic Medicine · 2019
Identification of Compound Heterozygous <i>EYS</i> Variants in a Korean Patient with Retinitis PigmentosaKim, Hyoung-Tae; Jang, Ja Hyun; Kang, Kyungeun; Ki, Chang-Seok; Chung, Hyewon · Laboratory Medicine Online · 2018
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100G. Rauh; H. Schuster; J. Fischer; Ch. Keller; G. Wolfram; N. Zöllner · 1991
Identification of a compound heterozygous mutation of ABCC2 in a patient with hyperbilirubinemiaXiang, Rong; Li, Jing-Jing; Fan, Liang-Liang; Jin, Jie-Yuan; Xia, Kun; Wang, Fang · Molecular Medicine Reports · 2017
Identification of Compound Heterozygous Mutation in a Korean Patient with Alpha 1-antitrypsin DeficiencyKo, Dae-Hyun; Chang, Ho Eun; Song, Sang Hoon; Yoon, Hoil; Park, Kyoung Un; Song, Junghan · The Korean Journal of Laboratory Medicine · 2011
Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigationsKanoun, Houda; Jarraya, Faiçal; Maalej, Bayen; Lahiani, Amina; Mahfoudh, Hichem; Makni, Fatma; Hachicha, Jamil; Fakhfakh, Faiza · BMC Nephrology · 2017
Identification of a novel compound heterozygous <i>IDUA</i> mutation underlies Mucopolysaccharidoses type I in a Chinese pedigreeZhou, Yong‐An; Li, Ping; Zhang, Yanping; Xiong, Qiuhong; Li, Chao; Zhao, Zhonghua; Wang, Yuxian; Xiao, Han · Molecular Genetics & Genomic Medicine · 2019
Issue InformationPhysiological Reports · 2013
Issue InformationPhysiological Reports · 2013
Issue InformationPhysiological Reports · 2013
CorrigendumPhysiological Reports · 2014
Issue InformationPhysiological Reports · 2014
CorrigendumPhysiological Reports · 2014
Issue InformationPhysiological Reports · 2014
Issue InformationPhysiological Reports · 2014