Results 241 to 250 of about 2,716,384 (302)

<i>PAPPA2</i> c.392G>C Heterozygous Mutation Associates Primary Open-Angle Glaucoma in a Chinese Family. [PDF]

Hum Mutat
Wang G, Guo Z, Ren J, Zhang G, Tao H, Liu Y, Zheng S, Zhang X, Wang D, Zhao R, Cui H, Zhu S, Xu H, Duan S, Li H.   +14 more
europepmc   +1 more source

Clinical Discovery and Molecular Analysis of Two Novel MSH2 Gene Mutations (p.Ala771Gly and p.Val797Gly) in Saudi Colorectal Cancer Patients: Potential Implications for Tumorigenesis. [PDF]

Health Sci Rep
Rasool M, Haque A, Alharthi M, Ali T, Karim S, Mira LS, Al-Abbasi F, Aljiffry M, Ghunaim M, Sibiany A, Pushparaj PN.   +10 more
europepmc   +1 more source

Whole exome sequencing identifies somatically mutated genes in bladder cancer: A pilot study from Bangladesh. [PDF]

Biochem Biophys Rep
Ahmed HU, Hosen MR, Mostofa MA, Hossain MA, Faruk MO, Shekhar HU, Hasan AM, Hosen MI.   +7 more
europepmc   +1 more source

Commentary: With Regards to the WISDOM trial. [PDF]

BJC Rep
Narod SA.
europepmc   +1 more source

A Pilot Study on Multigenic Thrombophilic Risk in Recurrent Pregnancy Loss: Interactions Between MTHFR Polymorphisms and Classical Thrombophilia-Associated SNPs. [PDF]

Int J Mol Sci
Badulescu OV, Hancianu M, Mircea C, Bojan A, Tesoi DF, Vladeanu MC, Ciocoiu M, Frasinariu OE, Plesoianu CE, Iliescu-Halitchi D, Bararu Bojan I.   +10 more
europepmc   +1 more source

A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile.

J Clin Endocrinol Metab
Rojas Velazquez MN, Lopez Dacal J, Jørgensen FS, Sanguineti N, Sharma K, Marino R, Pérez Garrido N, Vaiani E, Ramírez P, Scaglia P, Izquierdo A, Sansó G, Ropelato MG, Bergadá I, Rey RA, Grinspon RP, Pandey AV.   +16 more
europepmc   +1 more source