Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 4 (of 4 Records) |
Query Trace: Cri Du Chat Syndrome[original query] |
---|
8.5 Mb deletion at distal 5p in a male ascertained for azoospermia. American journal of medical genetics. Part A 2005 1 133A (2): 189-92. Rossi Elena, de Gregori Manuela, Grazia Patricelli Maria, Pramparo Tiziano, Argentiero Luisa, Giglio Sabrina, Sosta Katiuscia, Foresti Giovanni, Zuffardi Orset |
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes. American journal of obstetrics and gynecology 2015 Mar 212 (3): 332.e1-9. Wapner Ronald J, Babiarz Joshua E, Levy Brynn, Stosic Melissa, Zimmermann Bernhard, Sigurjonsson Styrmir, Wayham Nicholas, Ryan Allison, Banjevic Milena, Lacroute Phil, Hu Jing, Hall Megan P, Demko Zachary, Siddiqui Asim, Rabinowitz Matthew, Gross Susan J, Hill Matthew, Benn Pet |
F-FDG PET Identifies Altered Brain Metabolism in Patients with Cri du Chat Syndrome. Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2019 12 61 (8): 1195-1199. Cistaro Angelina, Quartuccio Natale, Piccardo Arnoldo, Fania Piercarlo, Spunton Marianna, Liava Alexandra, Danesino Cesare, Albani Giovanni, Guala Andr |
[Application analysis of noninvasive prenatal testing for fetal chromosome copy number variations in Chinese laboratories]. Zhonghua yi xue za zhi 2021 4 101 (15): 1088-1092. Shi J P, Tan P, Li J M, Zhang |
- Page last reviewed:Feb 1, 2024
- Content source: