PMC Articles for MedGen (Select 64512) - PMC

Links from MedGen

Items: 1 to 20 of 131

<< First< Prev

Page of 7

Select item 107073401.

Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome

Andrey V. Marakhonov, Tatyana A. Vasilyeva, Marina E. Minzhenkova, Natella V. Sukhanova, Peter A. Sparber, Natalya A. Andreeva, Margarita V. Teleshova, Fatima K.-M. Baybagisova, Nadezhda V. Shilova, Sergey I. Kutsev, Rena A. Zinchenko

Int J Mol Sci. 2023 Dec; 24(23): 16923. Published online 2023 Nov 29. doi: 10.3390/ijms242316923

PMCID:: PMC10707340

Article PDF–2.4M

Select item 103935332.

Transconjunctival XEN45 implantation for secondary open-angle glaucoma management in a pediatric patient with WAGR syndrome

Brooklyn Rawlyk, Mitchell D. Thatcher, Shehla Rubab, Maria Gabriela Campos-Baniak

Am J Ophthalmol Case Rep. 2023 Dec; 32: 101888. Published online 2023 Jul 7. doi: 10.1016/j.ajoc.2023.101888

PMCID:: PMC10393533

Article PDF–1.7M

Select item 101620953.

Visual Acuity in Aniridia and WAGR Syndrome

Michael A Krause, Kelly L Trout, James D Lauderdale, Peter A Netland

Clin Ophthalmol. 2023; 17: 1255–1261. Published online 2023 May 1. doi: 10.2147/OPTH.S405003

PMCID:: PMC10162095

Article PDF–1.0M

Select item 94084304.

Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases

Qiwei Wang, Xulin Zhang, Tingfeng Qin, Dongni Wang, Xiaoshan Lin, Yuanyuan Zhu, Haowen Tan, Lanqin Zhao, Jing Li, Zhuoling Lin, Haotian Lin, Weirong Chen

Genes (Basel) 2022 Aug; 13(8): 1431. Published online 2022 Aug 12. doi: 10.3390/genes13081431

PMCID:: PMC9408430

Article PDF–2.0M

Select item 87126935.

Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management

Kelly A. Duffy, Kelly L. Trout, Jennifer M. Gunckle, Shari McCullen Krantz, John Morris, Jennifer M. Kalish

Front Pediatr. 2021; 9: 733018. Published online 2021 Dec 14. doi: 10.3389/fped.2021.733018

PMCID:: PMC8712693

Article PDF–3.6M

Select item 83677326.

Sequences of COVID-19 in a child with WAGR syndrome: A case report

Sami Jomaa, Dana Shubat, Mamdoh AlTabban, Ibrahim Abdullah, Sawsan Ismail, Lina Khouri

Ann Med Surg (Lond) 2021 Sep; 69: 102732. Published online 2021 Aug 17. doi: 10.1016/j.amsu.2021.102732

PMCID:: PMC8367732

Article PDF–2.8M

Select item 78945347.

Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience

Janna A. Hol, Marjolijn C. J. Jongmans, Hélène Sudour‐Bonnange, Gema L. Ramírez‐Villar, Tanzina Chowdhury, Catherine Rechnitzer, Niklas Pal, Gudrun Schleiermacher, Axel Karow, Roland P. Kuiper, Beatriz de Camargo, Simona Avcin, Danka Redzic, Antonio Wachtel, Heidi Segers, Gordan M. Vujanic, Harm van Tinteren, Christophe Bergeron, Kathy Pritchard‐Jones, Norbert Graf, Marry M. van den Heuvel‐Eibrink, for the International Society of Pediatric Oncology Renal Tumor Study Group (SIOP‐RTSG)

Cancer. 2021 Feb 15; 127(4): 628–638. Published online 2020 Nov 4. doi: 10.1002/cncr.33304

PMCID:: PMC7894534

Article PDF–216K

Select item 73970888.

Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome

Tatyana A. Vasilyeva, Andrey V. Marakhonov, Natella V. Sukhanova, Sergey I. Kutsev, Rena A. Zinchenko

Genes (Basel) 2020 Jul; 11(7): 812. Published online 2020 Jul 17. doi: 10.3390/genes11070812

PMCID:: PMC7397088

Article PDF–453K

Select item 56540949.

Sustained endocrine profiles of a girl with WAGR syndrome

Yui Takada, Yasunari Sakai, Yuki Matsushita, Kazuhiro Ohkubo, Yuhki Koga, Satoshi Akamine, Michiko Torio, Yoshito Ishizaki, Masafumi Sanefuji, Hiroyuki Torisu, Chad A. Shaw, Masayo Kagami, Toshiro Hara, Shouichi Ohga

BMC Med Genet. 2017; 18: 117. Published online 2017 Oct 23. doi: 10.1186/s12881-017-0477-5

PMCID:: PMC5654094

Article PDF–626K

Select item 565317810.

Correction: The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene

Elizabeth D. Justice, Sarah J. Barnum, Thomas Kidd

PLoS Genet. 2017 Oct; 13(10): e1007061. Published online 2017 Oct 23. doi: 10.1371/journal.pgen.1007061

Corrects:: PLoS Genet. 2017 Aug; 13(8): e1006865.

PMCID:: PMC5653178

Correction PDF–278K

Select item 557849211.

The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene

Elizabeth D. Justice, Sarah J. Barnum, Thomas Kidd

PLoS Genet. 2017 Aug; 13(8): e1006865. Published online 2017 Aug 31. doi: 10.1371/journal.pgen.1006865

Correction in:: PLoS Genet. 2017 Oct; 13(10): e1007061.

PMCID:: PMC5578492

Article PDF–26M

Select item 532295212.

Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH

Fiona Blanco-Kelly, María Palomares, Elena Vallespín, Cristina Villaverde, Rubén Martín-Arenas, Camilo Vélez-Monsalve, Isabel Lorda-Sánchez, Julián Nevado, María José Trujillo-Tiebas, Pablo Lapunzina, Carmen Ayuso, Marta Corton

PLoS One. 2017; 12(2): e0172363. Published online 2017 Feb 23. doi: 10.1371/journal.pone.0172363

PMCID:: PMC5322952

Article PDF–1.7M

Select item 510384713.

Dysgerminoma developing from an ectopic ovary in a patient with WAGR syndrome: A case report

Rie Miura, Yoshihito Yokoyama, Tatsuhiko Shigeto, Masayuki Futagami, Hideki Mizunuma, Akira Kurose, Kazushi Tsuruga, Shinya Sasaki, Kiminori Terui, Etsuro Ito

Mol Clin Oncol. 2016 Nov; 5(5): 503–506. Published online 2016 Aug 25. doi: 10.3892/mco.2016.1004

PMCID:: PMC5103847

Article PDF–986K

Select item 464120214.

Prenatal Diagnosis of WAGR Syndrome

Berrin Tezcan, Philip Rich, Amarnath Bhide

Case Rep Obstet Gynecol. 2015; 2015: 928585. Published online 2015 Oct 28. doi: 10.1155/2015/928585

PMCID:: PMC4641202

Article PDF–922K

Select item 454347815.

Bezafibrate to prevent relapsing pancreatitis in WAGR syndrome

Daniela Diacono, Andrew Fagbemi, Joanne Puleston, Indraneel Banerjee

BMJ Case Rep. 2012; 2012: bcr2012006413. Published online 2012 Nov 14. doi: 10.1136/bcr-2012-006413

PMCID:: PMC4543478

Article PDF–225K

Select item 447438516.

A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning

Tadamichi Akagi, Munemitsu Yoshikawa, Hideo Nakanishi, Nagahisa Yoshimura

Clin Ophthalmol. 2015; 9: 1081–1084. Published online 2015 Jun 15. doi: 10.2147/OPTH.S80444

PMCID:: PMC4474385

Article PDF–822K

Select item 255370417.

Brain-Derived Neurotrophic Factor and Obesity in the WAGR Syndrome

Joan C. Han, Qing-Rong Liu, MaryPat Jones, Rebecca L. Levinn, Carolyn M. Menzie, Kyra S. Jefferson-George, Diane C. Adler-Wailes, Ethan L. Sanford, Felicitas L. Lacbawan, George R. Uhl, Owen M. Rennert, Jack A. Yanovski

N Engl J Med. Author manuscript; available in PMC 2008 Sep 28.

Published in final edited form as: N Engl J Med. 2008 Aug 28; 359(9): 918–927. doi: 10.1056/NEJMoa0801119

Correction in:: volume 359 on page 1414

PMCID:: PMC2553704

Article PDF–1.0M

Select item 105171118.

WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2)

J M McGaughran, H B Ward, D G R Evans

J Med Genet. 1995 Oct; 32(10): 823–824. doi: 10.1136/jmg.32.10.823

PMCID:: PMC1051711

Summary Page Browse PDF–351K

Select item 942167719.

Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review

Vanessa Sodré de Souza, Gabriela Corassa Rodrigues da Cunha, Beatriz R. Versiani, Claudiner Pereira de Oliveira, Maria Teresa Alves Silva Rosa, Silviene F. de Oliveira, Patricia N. Moretti, Juliana F. Mazzeu, Aline Pic-Taylor

Mol Syndromol. 2022 Jul; 13(4): 290–304. Published online 2022 Feb 11. doi: 10.1159/000518872

PMCID:: PMC9421677

Article PDF–533K

Select item 724594320.

Identification of a 6-month-old baby with a combination of WAGR and Potocki-Shaffer contiguous deletion syndromes by SNP array testing

Yan Meng, Jun Yang, Chan Tian, Jie Qiao

Hereditas. 2020; 157: 23. Published online 2020 May 23. doi: 10.1186/s41065-020-00132-2

PMCID:: PMC7245943

Article PDF–536K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from MedGen

Items: 1 to 20 of 131

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity