Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Counseling and PKD2[original query] |
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| [Study of two pedigrees affected with adult polycystic kidney disease and male infertility resulting from novel mutations of PKD1]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 6 35 (3): 376-379. Feng Zonggang, Wei Lei, Tan |
| Co-segregation of candidate polymorphism rs201204878 of the PKD1 gene in a large Iranian family with autosomal dominant polycystic disease. Experimental and therapeutic medicine 2019 Aug 18 (2): 1345-1349. Ranjzad Fariba, Tara Ahmad, Basiri Abbas, Aghdami Nasser, Moghadasali Re |
| Identification of missense and synonymous variants in Iranian patients suffering from autosomal dominant polycystic kidney disease. BMC nephrology 2020 9 21 (1): 408. Khadangi Fatemeh, Torkamanzehi Adam, Kerachian Mohammad Am |
| Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease. Genetics in medicine : official journal of the American College of Medical Genetics 2020 11 23 (4): 689-697. Durkie Miranda, Chong Jiehan, Valluru Manoj K, Harris Peter C, Ong Albert C |
| Polygenic risk affects the penetrance of monogenic kidney disease. medRxiv : the preprint server for health sciences 2023 5 . Atlas Khan, Ning Shang, Jordan G Nestor, Chunhua Weng, George Hripcsak, Peter C Harris, Ali G Gharavi, Krzysztof Kiryl |
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