Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Sleep and PHOX2B[original query] |
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Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE. Electrophoresis 2007 Mar 28 (6): 894-9. Hung Chia-Cheng, Su Yi-Ning, Tsao Po-Nien, Chen Pau-Chung, Lin Shio-Jean, Lin Cheng-Hui, Mu Shu-Chi, Liu Chieh-An, Chang Ying-Chao, Lin Win-Li, Hsieh Wu-Shiun, Hsu Su-Mi |
Obstructive sleep apnea syndrome (OSAS) in children with Class III malocclusion: involvement of the PHOX2B gene. Sleep & breathing = Schlaf & Atmung 2013 Dec 17 (4): 1275-80. Lavezzi Anna Maria, Casale Valentina, Oneda Roberta, Gioventù Silvia, Matturri Luigi, Farronato Giampiet |
That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS). International journal of legal medicine 2015 Sep 129 (5): 985-9. Poetsch Micaela, Todt Rebecca, Vennemann Mechtild, Bajanowski Thom |
Atypical presentations associated with non-polyalanine repeat PHOX2B mutations. American journal of medical genetics. Part A 2018 4 176 (7): 1627-1631. Katwa Umakanth, D'Gama Alissa M, Qualls Anita E, Donovan Lucas M, Heffernan Jody, Shi Jiahai, Agrawal Pankaj |
Sleep disturbances in parental caregivers and patients with congenital central hypoventilation syndrome. Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine 2022 12 . Finch Christina E, Leu Roberta M, Harford Kelli-Lee, Westbrook Adrianna L, Kasi Ajay |
Congenital Central Hypoventilation Syndrome: Diagnosis and Long-Term Ventilatory Outcomes. Clinical medicine insights. Pediatrics 2023 5 17 11795565231169556. Mary Ellen Fain, Adrianna L Westbrook, Ajay S Ka |
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- Page last updated:Apr 22, 2024
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