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Oct 26, 2019 (publication date) through May 1, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 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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Megan D. McCoy, Sara M. Sarasua, Jane M. DeLuca, Stephanie Davis, Katy Phelan, Roger Curtis Rogers, Luigi Boccuto. State of the Science for Kidney Disorders in Phelan-McDermid Syndrome: UPK3A, FBLN1, WNT7B, and CELSR1 as Candidate Genes. Genes 2022; 13(6): 1042 doi: 10.3390/genes13061042
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| 2 |
Hironori Bando, Shin Urai, Keitaro Kanie, Yuriko Sasaki, Masaaki Yamamoto, Hidenori Fukuoka, Genzo Iguchi, Sally A. Camper. Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing. Frontiers in Endocrinology 2022; 13 doi: 10.3389/fendo.2022.1008306
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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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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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