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Oct 26, 2019 (publication date) through Dec 24, 2025
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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
| Hu F, Sun L. Recognizable type of pituitary, heart, kidney and skeletal dysplasia mostly caused by SEMA3A mutation: A case report. World J Clin Cases 2019; 7(20): 3310-3315 [PMID: 31667184 DOI: 10.12998/wjcc.v7.i20.3310] |
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| ©2004-2025 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | Hu F, Sun L. Recognizable type of pituitary, heart, kidney and skeletal dysplasia mostly caused by SEMA3A mutation: A case report. World J Clin Cases 2019; 7(20): 3310-3315 [PMID: 31667184 DOI: 10.12998/wjcc.v7.i20.3310] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i20/3310.htm |
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| 2 |
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Riikka E. Mäkitie, Sanna Toiviainen-Salo, Ilkka Kaitila, Outi Mäkitie. A Novel Osteochondrodysplasia With Empty Sella Associates With a TBX2 Variant. Frontiers in Endocrinology 2022; 13 doi: 10.3389/fendo.2022.845889
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Hironori Bando, Shin Urai, Keitaro Kanie, Masaaki Yamamoto. Hypopituitarism: genetic, developmental, and acquired etiologies with a focus on the emerging concept of autoimmune hypophysitis. Endocrine Journal 2025; 72(6): 649 doi: 10.1507/endocrj.EJ25-0035
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Megan D. McCoy, Sara M. Sarasua, Jane M. DeLuca, Stephanie Davis, R. Curtis Rogers, Katy Phelan, Luigi Boccuto. Genetics of kidney disorders in Phelan-McDermid syndrome: evidence from 357 registry participants. Pediatric Nephrology 2024; 39(3): 749 doi: 10.1007/s00467-023-06146-y
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