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Jan-Philipp Bodenbender

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American Journal of Ophthalmology|June 23, 2024
Clinical and Genetic Findings in a Cohort of Patients with PRPF31-Associated Retinal DystrophyJan-Philipp Bodenbender, Leon Bethge, Katarina Stingl, et al.
International Journal of Molecular Sciences|February 11, 2023
Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal DystrophyJan-Philipp Bodenbender, Valerio Marino, Leon Bethge, et al.
Acta Ophthalmologica|June 26, 2026
Clinical manifestations of dual-gene variants in retinitis pigmentosaLasse Wolfram, Jan-Philipp Bodenbender, David A Merle, et al.
Scientific Reports|May 8, 2024
Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypesJan-Philipp Bodenbender, Valerio Marino, Julia Philipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2025
Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathyAnneke T Vulto-van Silfhout, Ingrid M Jazet, Suzanne Yzer, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
American Journal of Ophthalmology|June 23, 2024
Clinical and Genetic Findings in a Cohort of Patients with PRPF31-Associated Retinal DystrophyJan-Philipp Bodenbender, Leon Bethge, Katarina Stingl, et al.
International Journal of Molecular Sciences|February 11, 2023
Biallelic Variants in TULP1 Are Associated with Heterogeneous Phenotypes of Retinal DystrophyJan-Philipp Bodenbender, Valerio Marino, Leon Bethge, et al.
Acta Ophthalmologica|June 26, 2026
Clinical manifestations of dual-gene variants in retinitis pigmentosaLasse Wolfram, Jan-Philipp Bodenbender, David A Merle, et al.
Scientific Reports|May 8, 2024
Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypesJan-Philipp Bodenbender, Valerio Marino, Julia Philipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2025
Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathyAnneke T Vulto-van Silfhout, Ingrid M Jazet, Suzanne Yzer, et al.
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