Autor: JMG Online First
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Correction: UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants
Tsoulaki O, Evans DG, Sinha K, et al. UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants. Journal of Medical Genetics 2025;62:559-565.The name of author Farrah S Bakr has been corrected. Both the…
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Correction: UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants
Tsoulaki O, Evans DG, Sinha K, et al. UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants. Journal of Medical Genetics 2025;62:559-565.The name of author Farrah S Bakr has been corrected. Both the…
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Retraction: multiple articles in volume 56, issue 1 (2019)
Seven research papers and one editorial submitted in response to a call for papers on and published in a topic collection ‘Genomic aspects of cancer immunotherapy: Challenges and clinical implications’ in the Journal of Medical Genetics are…
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Retraction: multiple articles in volume 56, issue 1 (2019)
Seven research papers and one editorial submitted in response to a call for papers on and published in a topic collection ‘Genomic aspects of cancer immunotherapy: Challenges and clinical implications’ in the Journal of Medical Genetics ar…
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Retraction: multiple articles in volume 56, issue 1 (2019)
Seven research papers and one editorial submitted in response to a call for papers on and published in a topic collection ‘Genomic aspects of cancer immunotherapy: Challenges and clinical implications’ in the Journal of Medical Genetics ar…
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Correction 2: A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct
On the last 3 rows/lines (subjects 2106, 2107, 2108) of table 4 on page 670, the Allele 1 genotype «p.Asp324Tyr» should be «p.Asn324Tyr». This error does not change, in any way, the conclusions of the paper.
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Correction: SETD1B-associated neurodevelopmental disorder
Roston A, Evans D, Gill H et al, EPGEN Study. SETD1B-associated neurodevelopmental disorder. J Med Genet 2021;58:196–204. doi: 10.1136/jmedgenet-2019-106756There is a typographical error in Individual 3’s reported nucleotide sequence. Curre…