| P50 | author | Kin-Mang Lau | Q58469938 |
| P2093 | author name string | Wai-Shan Wong | |
| | Margaret H L Ng | |
| | Natalie P H Chan | |
| | Nelson C N Chan | |
| | Eudora Y D Chow | |
| | Michael L G Wong | |
| | Chi-Keung Cheng | |
| | Connie M L Wong | |
| | Joyce H Y Kwong | |
| | Kelvin C F Chan | |
| | Raymond W Chu | |
| | Rosalina K L Ip | |
| P2860 | cites work | Genetic structure of the Han Chinese population revealed by genome-wide SNP variation | Q24644546 |
| | A method and server for predicting damaging missense mutations | Q27860835 |
| | Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 |
| | Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I. | Q34124313 |
| | Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population | Q37618937 |
| | Protein S abnormalities: a diagnostic nightmare | Q37869445 |
| | Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis | Q40032861 |
| | Genetic predisposition of white matter infarction with protein S deficiency and R355C mutation | Q42775128 |
| | Molecular basis of protein S deficiency in China. | Q46023682 |
| | PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency. | Q50924493 |
| | A novel PROS1 mutation, c.74dupA, was identified in a protein S deficiency family. | Q51326237 |
| | Molecular basis of protein S deficiency. | Q55044585 |
| | Protein S and C4b-binding protein: components involved in the regulation of the protein C anticoagulant system | Q55049170 |
| | Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene | Q61835634 |
| | Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants | Q73734728 |
| | An Sp1 binding site mutation of the PROS1 promoter in a patient with protein S deficiency | Q80537800 |
| | PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations | Q81149769 |
| | Protein S-K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients | Q82484437 |
| | Genotype and laboratory and clinical phenotypes of protein s deficiency | Q83286423 |
| | Venous thromboembolism in Asia--an unrecognised and under-treated problem? | Q84743894 |
| P433 | issue | 1 | |
| P304 | page(s) | 120-124 | |
| P577 | publication date | 2018-07-01 | |
| P1433 | published in | Journal of Thrombosis and Thrombolysis | Q15766541 |
| P1476 | title | Distinctive regional-specific PROS1 mutation spectrum in Southern China | |
| P478 | volume | 46 | |