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Cited by in CrossRef
For: Li Y, Zhou Z, Xu Y, Wang ZR. Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities in an 18.5-mo-old boy: A case report. World J Clin Cases 2023; 11(16): 3891-3898 [PMID: 37383123 DOI: 10.12998/wjcc.v11.i16.3891]
URL: https://www.wjgnet.com/2307-8960/full/v11/i16/3891.htm
Number Citing Articles
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Davide Politano, Francesca Marazzi, Ilaria Scognamillo, Federica Morelli, Sabrina Signorini, Simone Gana, Silvia Nicolosi, Elisa Rognone, Renato Borgatti, Enza Maria Valente, Romina Romaniello. A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literatureBrain and Development 2025; 47(3): 104351 doi: 10.1016/j.braindev.2025.104351