Long read sequencing and expression studies of AHDC1 deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism

Overview of attention for article published in Human Mutation, September 2022

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nanopore: Long Read Sequencing and Expression Studies of AHDC1 Deletions in Xia-Gibbs Syndrome Reveal a Novel Genetic Regulatory Mechanism https://t.co/1ahVNSVMal

Long Read Sequencing and Expression Studies of AHDC1 Deletions in Xia-Gibbs Syndrome Reveal a Novel Genetic Regulatory Mechanism https://t.co/I6axi5czEr https://t.co/oAfTdP7eMh

Long Read Sequencing and Expression Studies of AHDC1 Deletions in Xia-Gibbs Syndrome Reveal a Novel Genetic Regulatory Mechanism https://t.co/4AZKwh8MDG https://t.co/qVEz7N9PAB

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