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4 in total

1. Sleep and neurobehavioral characteristics of 5- to 7-year-old children with parentally reported symptoms of attention-deficit/hyperactivity disorder.

Authors: Louise M O'Brien; Cheryl R Holbrook; Carolyn B Mervis; Carrie J Klaus; Jennifer L Bruner; Troy J Raffield; Jennifer Rutherford; Rochelle C Mehl; Mei Wang; Andrew Tuell; Brittany C Hume; David Gozal
Journal: Pediatrics Date: 2003-03 Impact factor: 7.124

2. FOXP1 mutations cause intellectual disability and a recognizable phenotype.

Authors: Anna K Le Fevre; Sharelle Taylor; Neva H Malek; Denise Horn; Christopher W Carr; Omar A Abdul-Rahman; Sherindan O'Donnell; Trent Burgess; Marie Shaw; Jozef Gecz; Nicole Bain; Kerry Fagan; Matthew F Hunter
Journal: Am J Med Genet A Date: 2013-09-24 Impact factor: 2.802

3. A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis.

Authors: Mitchel J Pariani; Andrew Spencer; John M Graham; David L Rimoin
Journal: Eur J Med Genet Date: 2009-03-28 Impact factor: 2.708

4. Prospective investigation of FOXP1 syndrome.

Authors: Paige M Siper; Silvia De Rubeis; Alexander Kolevzon; Joseph D Buxbaum; Maria Del Pilar Trelles; Allison Durkin; Daniele Di Marino; François Muratet; Yitzchak Frank; Reymundo Lozano; Evan E Eichler; Morgan Kelly; Jennifer Beighley; Jennifer Gerdts; Arianne S Wallace; Heather C Mefford; Raphael A Bernier
Journal: Mol Autism Date: 2017-10-24 Impact factor: 7.509

4 in total