# Search results for: Hossein Jafari

Annals of Human Genetics > 86 > 1 > 52 - 62

**Background**: Gabriele‐de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in

*YY1*. In this study, we report a 10‐year‐old boy with a de novo novel pathogenic variant in

*YY1*, the first Iranian patient with Gabriele‐de Vries Syndrome.

**Methods**: The novel de novo pathogenic variant detected in this study (NM_003403:c.690delA, p.Glu231Ilefs*25) was identified...

Mathematical Methods in the Applied Sciences > 45 > 2 > 1033 - 1062

Polymers for Advanced Technologies > 32 > 10 > 3948 - 3954

Numerical Methods for Partial Differential Equations > 37 > 2 > 1397 - 1406

Advances in Difference Equations > 2019 > 2019 > 1 > 1-10

Journal of Optimization Theory and Applications > 2019 > 183 > 2 > 688-704

Biotechnology Letters > 2019 > 41 > 6-7 > 691-700

Mathematical Methods in the Applied Sciences > 42 > 7 > 2334 - 2343

Advances in Difference Equations > 2019 > 2019 > 1 > 1-11

Molecular Biology Reports > 2019 > 46 > 1 > 1069-1078

*Ferula pseudalliacea*) and sweet (

*Ferula assa-foetida*) asafetida (Apiaceae family) are well-known economic and medicinal herbs owing to their gum. This study investigates genetic differentiation of

*F. pseudalliacea*and

*F. assa-foetida*using ISSR markers, to determine the effective primer and to assess the possibility of separating sweet and bitter plant populations from each other. Results...

Bulletin of the Iranian Mathematical Society > 2019 > 45 > 4 > 1105-1116

*G*will be given in order the group

*G*to have a unique, and necessarily cyclic, subgroup of order

*m*, where

*m*is a fixed divisor of |

*G*|. These conditions are about “the number of cyclic subgroups of particular orders” and “the number of elements of particular orders”.

Mathematical Methods in the Applied Sciences > 41 > 18 > 9134 - 9141

Journal of Materials Science: Materials in Electronics > 2018 > 29 > 24 > 20639- 20649

Congenital Heart Disease > 13 > 2 > 295 - 304

*GATA4*gene induce inherited atrial and ventricular septation defects, which is the most frequent forms of congenital heart defects (CHDs) constituting about half of all cases. Method We have performed High resolution melting (HRM) mutation scanning of

*GATA4*coding exons of nonsyndrome 100 patients as a case group including 39 atrial septal defects (ASD), 57 ventricular...

Applied Surface Science > 2018 > 427 > PA > 496-506

Physics Letters A > 2017 > 381 > 34 > 2813-2820

Concurrency and Computation: Practice and Experience > 29 > 17 > n/a - n/a

Optik - International Journal for Light and Electron Optics > 2017 > 139 > C > 72-76

International Journal of Computer Assisted Radiology and Surgery > 2017 > 12 > 6 > 1021-1030