| 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] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i16/3891.htm |
| Number | Citing Articles |
| 1 |
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 literature. Brain and Development 2025; 47(3) doi: 10.1016/j.braindev.2025.104351
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| 2 |
Tatjana Damnjanovic, Nela Maksimovic, Ana Djuranovic Uklein, Brankica Bosankic, Biljana Jekic, Milka Grk, Marija Dusanovic Pjevic, Milica Rasic, Natasa Stojanovski, Milica Pesic, Ivana Novakovic, Goran Cuturilo, Dijana Perović. Analysis of Copy Number and Sequence Variants Linked to Cardiac Development in Children with Syndromic Congenital Heart Defects. Cardiogenetics 2026; 16(2) doi: 10.3390/cardiogenetics16020013
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| 3 |
Nurana Mammadova, Nihal Hatipoglu, Munis Dundar. A novel de novo frameshift variant in ZMYM2 expands the neuropsychiatric spectrum of NECRC syndrome: a case report. Molecular Biology Reports 2026; 53(1) doi: 10.1007/s11033-026-11841-8
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