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malformation相关文献:
A systematic review of maternal diabetes and congenital skeletal malformation.
Shah K, Shah H.
Congenit Anom (Kyoto). 2022 May;62(3):113-122. doi: 10.1111/cga.12463. Epub 2022 Mar 30.
PMID:35319786
Congenital pulmonary airway malformation: advances and controversies.
Wong KKY, Flake AW, Tibboel D, Rottier RJ, Tam PKH.
Lancet Child Adolesc Health. 2018 Apr;2(4):290-297. doi: 10.1016/S2352-4642(18)30035-X. Epub 2018 Feb 17.
PMID:30169300
Hirschsprung disease and anorectal malformation.
Wetherill C, Sutcliffe J.
Early Hum Dev. 2014 Dec;90(12):927-32. doi: 10.1016/j.earlhumdev.2014.09.016. Epub 2014 Oct 22.
PMID:25448783
[Malformation and plastic surgery in childhood].
Siegert R, Magritz R.
Laryngorhinootologie. 2014 Mar;93 Suppl 1:S203-17. doi: 10.1055/s-0033-1363658. Epub 2014 Apr 7.
PMID:24710784
Fifty years of recognizable patterns of human malformation: Insights and opportunities.
Innes AM, Lynch DC.
Am J Med Genet A. 2021 Sep;185(9):2653-2669. doi: 10.1002/ajmg.a.62240. Epub 2021 May 5.
PMID:33951288
Arteriovenous malformation phenotype resembling congenital hemangioma contains KRAS mutations.
Sudduth CL, McGuire AM, Smits PJ, Konczyk DJ, Al-Ibraheemi A, Fishman SJ, Greene AK.
Clin Genet. 2020 Dec;98(6):595-597. doi: 10.1111/cge.13833. Epub 2020 Sep 2.
PMID:32799314
Anorectal malformation associated with delayed presentation of right Bochdalek type diaphragmatic hernia.
Fourie N, De Vos C, Le Roux CE, Goussard P.
BMJ Case Rep. 2022 Jul 26;15(7):e249980. doi: 10.1136/bcr-2022-249980.
PMID:35882437
Congenital malformation in green turtle embryos and hatchlings.
Sönmez B, Sağol Ö.
J Exp Zool A Ecol Integr Physiol. 2024 Oct;341(8):925-936. doi: 10.1002/jez.2851. Epub 2024 Jul 2.
PMID:38953157
Implementation of auricular malformation screenings in the newborn population.
Liu YC, Kini S, Barton G, Pham T, Marcet-Gonzalez J, Novak B.
Int J Pediatr Otorhinolaryngol. 2020 Jun;133:109999. doi: 10.1016/j.ijporl.2020.109999. Epub 2020 Mar 12.
PMID:32224391
Laryngo-tracheo-oesophageal clefts.
Leboulanger N, Garabédian EN.
Orphanet J Rare Dis. 2011 Dec 7;6:81. doi: 10.1186/1750-1172-6-81.
PMID:22151899
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