Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 5 (of 5 Records) |
| Query Trace: Wagr Syndrome[original query] |
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| WT1 gene analysis in sporadic early-onset and bilateral wilms tumor patients without associated abnormalities. Journal of pediatric hematology/oncology 2005 Apr 27 (4): 197-201. Perotti Daniela, Mondini Patrizia, Terenziani Monica, Spreafico Filippo, Collini Paola, Fossati-Bellani Franca, Radice Pao |
| Brain-derived neurotrophic factor and obesity in the WAGR syndrome. The New England journal of medicine 2008 Aug 359 (9): 918-27. Han Joan C, Liu Qing-Rong, Jones MaryPat, Levinn Rebecca L, Menzie Carolyn M, Jefferson-George Kyra S, Adler-Wailes Diane C, Sanford Ethan L, Lacbawan Felicitas L, Uhl George R, Rennert Owen M, Yanovski Jack |
| Rare Syndromes and Common Variants of the Brain-Derived Neurotrophic Factor Gene in Human Obesity. Progress in molecular biology and translational science 2016 140 75-95. Han J |
| A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977?kb deletion in the 11p13 region. BMC medical genomics 2020 9 13 (Suppl 8): 130. Vasilyeva Tatyana A, Marakhonov Andrey V, Minzhenkova Marina E, Markova Zhanna G, Petrova Nika V, Sukhanova Natella V, Koshkin Philipp A, Pyankov Denis V, Kanivets Ilya V, Korostelev Sergey A, Krynskaya Irina A, Shilova Nadezhda V, Kutsev Sergey I, Kadyshev Vitaly V, Zinchenko Rena |
| Visual Acuity in Aniridia and WAGR Syndrome. Clinical ophthalmology (Auckland, N.Z.) 2023 5 17 1255-1261. Michael A Krause, Kelly L Trout, James D Lauderdale, Peter A Netla |
- Page last reviewed:Feb 1, 2024
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