| scholarly article | Q13442814 |
| P2093 | author name string | Chalinee Monsereenusorn | |
| Chanchai Traivaree | |||
| Boonchai Boonyawat | |||
| Arunotai Meekaewkunchorn | |||
| Premsak Laoyookhong | |||
| Saranya Suwansingh | |||
| P2860 | cites work | Prenatal Exclusion of Severe Factor VII Deficiency | Q57263831 |
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| Ultrasonography and possible ruptured abdominal aortic aneurysms | Q66942287 | ||
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| Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency | Q73786779 | ||
| Twenty two novel mutations of the factor VII gene in factor VII deficiency | Q73912612 | ||
| Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients | Q80557117 | ||
| Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation | Q22254871 | ||
| A cell-based model of hemostasis | Q28204461 | ||
| Characterization of a cDNA coding for human factor VII | Q28646329 | ||
| Intracranial and extracranial hemorrhages in newborns with hemophilia: a review of the literature | Q33710505 | ||
| Factor VII deficiency and the FVII mutation database | Q34119225 | ||
| Recessively inherited coagulation disorders. | Q35770792 | ||
| Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant. | Q37209107 | ||
| Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII. | Q40278893 | ||
| Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene | Q45107661 | ||
| Current practices regarding newborn intracranial haemorrhage and obstetrical care and mode of delivery of pregnant haemophilia carriers: a survey of obstetricians, neonatologists and haematologists in the United States, on behalf of the National Hem | Q45863766 | ||
| Prophylactic effect of recombinant factor VIIa with congenital factor VII deficiency | Q45876654 | ||
| Clinical picture and management of congenital factor VII deficiency | Q45878804 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 3.0 Unported | Q18810331 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P921 | main subject | factor VII deficiency | Q18555032 |
| P304 | page(s) | 37-41 | |
| P577 | publication date | 2017-06-21 | |
| P1433 | published in | The Application of Clinical Genetics | Q15817525 |
| P1476 | title | Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children | |
| P478 | volume | 10 |
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