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Saeed Reza Ghaffari

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Ophthalmic Genetics|November 18, 2021
Identification of a novel de novo variant in <i>OTX2</i> in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosisMaryam Rafati, Faezeh Mohamadhashem, Koosha Jalilian, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 16, 2013
Correlation of nuchal translucency and thyroxine at 11-13 weeks of gestationSedigheh Hantoushzadeh, Fatemeh Tara, Bahram Salmanian, et al.
Archives of Dermatological Research|December 7, 2023
Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosisMitra Chegini, Maryam Eslami, Mahsa Motavaf, et al.
Plos One|November 23, 2013
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophiesTobias Eisenberger, Christine Neuhaus, Arif O Khan, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Ophthalmic Genetics|November 18, 2021
Identification of a novel de novo variant in <i>OTX2</i> in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosisMaryam Rafati, Faezeh Mohamadhashem, Koosha Jalilian, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 16, 2013
Correlation of nuchal translucency and thyroxine at 11-13 weeks of gestationSedigheh Hantoushzadeh, Fatemeh Tara, Bahram Salmanian, et al.
Archives of Dermatological Research|December 7, 2023
Whole exome sequencing identifies novel pathogenic variants in TGM1 and ALOX12B in patients with hereditary ichthyosisMitra Chegini, Maryam Eslami, Mahsa Motavaf, et al.
Plos One|November 23, 2013
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophiesTobias Eisenberger, Christine Neuhaus, Arif O Khan, et al.
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