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Sateesh Maddirevula

Showing results (11-20 of 78) with videos related to

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Journal of Assisted Reproduction and Genetics|February 14, 2022
Recurrent spontaneous oocyte activation causes female infertilitySerdar Coskun, Sateesh Maddirevula, Khalid Awartani, et al.
Med (New York, N.Y.)|July 24, 2024
NanoRanger enables rapid single-base-pair resolution of genomic disordersYingzi Zhang, Chongwei Bi, Seba Nadeef, et al.
Human Genetics|October 27, 2021
ASTL is mutated in female infertilitySateesh Maddirevula, Serdar Coskun, Mashael Al-Qahtani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Increasing the sensitivity of clinical exome sequencing through improved filtration strategyHanan E Shamseldin, Sateesh Maddirevula, Eissa Faqeih, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
Confirming the involvement of PIEZO2 in the etiology of Marden-Walker syndromeMohammed Zain Seidahmed, Sateesh Maddirevula, Abeer M Miqdad, et al.
European Journal of Medical Genetics|March 24, 2020
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severityAmira Nabil, Sahar El Shafei, Nihal M El Shakankiri, et al.
Clinical Genetics|January 20, 2026
Biallelic STEAP3 Variant in Neonatal Hemophagocytic LymphohistiocytosisAbdullah H Alfalah, Mohamed Y Elsaid, Ahmed Alrajjal, et al.
Human Genetics|November 10, 2021
Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variantSateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics|March 16, 2020
A genomics approach to females with infertility and recurrent pregnancy lossSateesh Maddirevula, Khalid Awartani, Serdar Coskun, et al.
American Journal of Human Genetics|October 3, 2017
Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2Sateesh Maddirevula, Serdar Coskun, Saad Alhassan, et al.
Pageof 8

Showing results (11-20 of 78) with videos related to

Sort By:
Pageof 8
Journal of Assisted Reproduction and Genetics|February 14, 2022
Recurrent spontaneous oocyte activation causes female infertilitySerdar Coskun, Sateesh Maddirevula, Khalid Awartani, et al.
Med (New York, N.Y.)|July 24, 2024
NanoRanger enables rapid single-base-pair resolution of genomic disordersYingzi Zhang, Chongwei Bi, Seba Nadeef, et al.
Human Genetics|October 27, 2021
ASTL is mutated in female infertilitySateesh Maddirevula, Serdar Coskun, Mashael Al-Qahtani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Increasing the sensitivity of clinical exome sequencing through improved filtration strategyHanan E Shamseldin, Sateesh Maddirevula, Eissa Faqeih, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
Confirming the involvement of PIEZO2 in the etiology of Marden-Walker syndromeMohammed Zain Seidahmed, Sateesh Maddirevula, Abeer M Miqdad, et al.
European Journal of Medical Genetics|March 24, 2020
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severityAmira Nabil, Sahar El Shafei, Nihal M El Shakankiri, et al.
Clinical Genetics|January 20, 2026
Biallelic STEAP3 Variant in Neonatal Hemophagocytic LymphohistiocytosisAbdullah H Alfalah, Mohamed Y Elsaid, Ahmed Alrajjal, et al.
Human Genetics|November 10, 2021
Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variantSateesh Maddirevula, Seham Alameer, Nour Ewida, et al.
Human Genetics|March 16, 2020
A genomics approach to females with infertility and recurrent pregnancy lossSateesh Maddirevula, Khalid Awartani, Serdar Coskun, et al.
American Journal of Human Genetics|October 3, 2017
Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2Sateesh Maddirevula, Serdar Coskun, Saad Alhassan, et al.
Pageof 8