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Jul 6, 2023 (publication date) through Feb 7, 2026
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| Li J, Chen LN, He HL. CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature. World J Clin Cases 2023; 11(19): 4655-4663 [PMID: 37469742 DOI: 10.12998/wjcc.v11.i19.4655] |
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| ©2004-2026 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | Li J, Chen LN, He HL. CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature. World J Clin Cases 2023; 11(19): 4655-4663 [PMID: 37469742 DOI: 10.12998/wjcc.v11.i19.4655] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i19/4655.htm |
| Number | Citing Articles |
| 1 |
Uttara Kurup, David B N Lim, Helena Palau, Avinaash V Maharaj, Miho Ishida, Justin H Davies, Helen L Storr. Approach to the Patient With Suspected Silver-Russell Syndrome. The Journal of Clinical Endocrinology & Metabolism 2024; 109(10): e1889 doi: 10.1210/clinem/dgae423
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| 2 |
Uttara Kurup, David B. N. Lim, Avinaash V. Maharaj, Miho Ishida, Justin H. Davies, Helen L. Storr. Silver-Russell syndrome secondary to rare (epi)genotypes exhibits phenotypic heterogeneity challenging clinical diagnosis. Clinical Epigenetics 2025; 17(1) doi: 10.1186/s13148-025-02023-7
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| 3 |
Ekaterina Kim, Anastasiia Lavreniuk, Olga Spasskaya, Anna Eremkina, Rustam Salimkhanov, Liliya Urusova, Natalia Tarbaeva, Sergey Popov, Victoria Zakharova, Natalia Mokrysheva. Case report: Relapse of intrathyroidal parathyroid carcinoma in a patient with novel variants in MET and CDKN1C genes. Frontiers in Oncology 2025; 14 doi: 10.3389/fonc.2024.1441083
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| 4 |
Yena Lee, Hwal Rim Jeong, Eun Young Kim, Eu-Seon Noh, Hye Young Jin, Eun Byul Kwon, Hye Jin Lee, Sang Hee Park, Young-Jun Seo, Go Hun Seo, Su Jin Kim, Ji-Eun Lee, Nan Young Kim, Sangkyoon Hong, Min Jae Kang, Il Tae Hwang. Genomic Insights into Short Stature in Children Born Small for Gestational Age: A Korean Multicenter Exome Study. The Journal of Clinical Endocrinology & Metabolism 2025; doi: 10.1210/clinem/dgaf533
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| 5 |
Alessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella, Sara Guzzetti, Luciano Calzari, Lara Branca, Melissa Bellini, Lidia Larizza, Flavia Napoli, Anna Elsa Maria Allegri, Mohamad Maghnie, Silvia Russo. PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion. Scientific Reports 2025; 15(1) doi: 10.1038/s41598-025-32983-y
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