Congenital Hemolytic Anemia.
Haley K.
Med Clin North Am. 2017 Mar;101(2):361-374. doi: 10.1016/j.mcna.2016.09.008. Epub 2016 Dec 8.
Extracorporeal Membrane Oxygenation for Hemodynamic Support.
Straube T, Cheifetz IM, Jackson KW.
Clin Perinatol. 2020 Sep;47(3):671-684. doi: 10.1016/j.clp.2020.05.016. Epub 2020 May 26.
Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects.
Werren EA, Rodriguez Bey G, Majethia P, Kaur P, Patil SJ, Kekatpure MV, Afenjar A, Qebibo L, Burglen L, Tomoum H, Demurger F, Duborg C, Siddiqui S, Tsan YC, Abdullah U, Ali Z, Saadi SM, Baig SM, Houlden H, Maroofian R, Padiath QS, Bielas SL, Shukla A.
Brain. 2024 Dec 3;147(12):4033-4042. doi: 10.1093/brain/awae299.
Segmental colonic length and mobility.
Phillips M, Patel A, Meredith P, Will O, Brassett C.
Ann R Coll Surg Engl. 2015 Sep;97(6):439-44. doi: 10.1308/003588415X14181254790527. Epub 2015 Aug 14.
Chevalier Jackson Lecture. Congenital laryngeal webs.
Benjamin B.
Ann Otol Rhinol Laryngol. 1983 Jul-Aug;92(4 Pt 1):317-26. doi: 10.1177/000348948309200401.
Early repair of congenital diaphragmatic hernia on extracorporeal membrane oxygenation.
Dassinger MS, Copeland DR, Gossett J, Little DC, Jackson RJ, Smith SD; Congenital Diaphragmatic Hernia Study Group.
J Pediatr Surg. 2010 Apr;45(4):693-7. doi: 10.1016/j.jpedsurg.2009.08.011.
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations.
Peron A, D'Arco F, Aldinger KA, Smith-Hicks C, Zweier C, Gradek GA, Bradbury K, Accogli A, Andersen EF, Au PYB, Battini R, Beleford D, Bird LM, Bouman A, Bruel AL, Busk ØL, Campeau PM, Capra V, Carlston C, Carmichael J, Chassevent A, Clayton-Smith J, Bamshad MJ, Earl DL, Faivre L, Philippe C, Ferreira P, Graul-Neumann L, Green MJ, Haffner D, Haldipur P, Hanna S, Houge G, Jones WD, Kraus C, Kristiansen BE, Lespinasse J, Low KJ, Lynch SA, Maia S, Mao R, Kalinauskiene R, Melver C, McDonald K, Montgomery T, Morleo M, Motter C, Openshaw AS, Palumbos JC, Parikh AS, Perilla-Young Y, Powell CM, Person R, Desai M, Piard J, Pfundt R, Scala M, Serey-Gaut M, Shears D, Slavotinek A, Suri M, Turner C, Tvrdik T, Weiss K, Wentzensen IM, Zollino M, Hsieh TC; C4RCD Research Group; Telethon Undiagnosed Disease Program (TUDP); University of Washington Center for Mendelian Genomics (UW-CMG); de Vries BBA, Guillemot F, Dobyns WB, Viskochil D, Dias C.
Eur J Hum Genet. 2025 Mar;33(3):312-324. doi: 10.1038/s41431-024-01701-z. Epub 2024 Oct 24.
Congenital syphilis: the University of Miami/Jackson Memorial Medical Center experience, 1986-1988.
Ricci JM, Fojaco RM, O'Sullivan MJ.
Obstet Gynecol. 1989 Nov;74(5):687-93.
Memory Problems in Children With Congenital Heart Disease: A Narrative Review.
Jackson WM, Monteleone M, Kim A, Ko R.
J Neurosurg Anesthesiol. 2023 Jan 1;35(1):136-141. doi: 10.1097/ANA.0000000000000880. Epub 2022 Dec 6.
Complex genetics of glaucoma susceptibility.
Libby RT, Gould DB, Anderson MG, John SW.
Annu Rev Genomics Hum Genet. 2005;6:15-44. doi: 10.1146/annurev.genom.6.080604.162209.
