Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015.
Shay JW, Homma N, Zhou R, Naseer MI, Chaudhary AG, Al-Qahtani M, Hirokawa N, Goudarzi M, Fornace AJ Jr, Baeesa S, Hussain D, Bangash M, Alghamdi F, Schulten HJ, Carracedo A, Khan I, Qashqari H, Madkhali N, Saka M, Saini KS, Jamal A, Al-Maghrabi J, Abuzenadah A, Chaudhary A, Al Qahtani M, Damanhouri G, Alkhatabi H, Goodeve A, Crookes L, Niksic N, Beauchamp N, Abuzenadah AM, Vaught J, Budowle B, Assidi M, Buhmeida A, Al-Maghrabi J, Buhmeida A, Assidi M, Merdad L, Kumar S, Miura S, Gomez K, Carracedo A, Rasool M, Rebai A, Karim S, Eldin HFN, Abusamra H, Alhathli EM, Salem N, Al-Qahtani MH, Kumar S, Faheem H, Agarwa A, Nieschlag E, Wistuba J, Damm OS, Beg MA, Abdel-Meguid TA, Mosli HA, Bajouh OS, Abuzenadah AM, Al-Qahtani MH, Coskun S, Abu-Elmagd M, Buhmeida A, Dallol A, Al-Maghrabi J, Hakamy S, Al-Qahtani W, Al-Harbi A, Hussain S, Assidi M, Al-Qahtani M, Abuzenadah A, Ozkosem B, DuBois R, Messaoudi SS, Dandana MT, Mahjoub T, Almawi WY, Abdalla S, Al-Aama MN, Elzawahry A, Takahashi T, Mimaki S, Furukawa E, Nakatsuka R, Kurosaka I, Nishigaki T, Nakamura H, Serada S, Naka T, Hirota S, Shibata T, Tsuchihara K, Nishida T, Kato M, Mehmood S, Ashraf NM, Asif A, Bilal M, Mehmood MS, Hussain …
BMC Genomics. 2016 Jul 20;17 Suppl 6(Suppl 6):487. doi: 10.1186/s12864-016-2858-0.
Hereditary Nephrogenic Diabetes Insipidus.
Knoers N, Lemmink H.
2000 Feb 12 [updated 2020 Feb 27]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
Pregnancy in women with Alport syndrome.
Crovetto F, Moroni G, Zaina B, Acaia B, Ossola MW, Fedele L.
Int Urol Nephrol. 2013 Aug;45(4):1223-7. doi: 10.1007/s11255-012-0154-8. Epub 2012 Mar 15.
Neonatal Life-Threatening Nonoliguric Hyperkalemia Under Therapeutic Hypothermia.
Piastra M, Tempera A, De Carolis MP, Pezza L, Genovese O, Benassi C, Morena TC, Picconi E, Zito G, De Rosa G, Conti G, De Luca D.
Ther Hypothermia Temp Manag. 2021 Dec;11(4):238-241. doi: 10.1089/ther.2021.0009. Epub 2021 Aug 17.
Update on the Prenatal Diagnosis and Outcomes of Fetal Bilateral Renal Agenesis.
Huber C, Shazly SA, Blumenfeld YJ, Jelin E, Ruano R.
Obstet Gynecol Surv. 2019 May;74(5):298-302. doi: 10.1097/OGX.0000000000000670.
Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
Su J, Qin Z, Fu H, Luo J, Huang Y, Huang P, Zhang S, Liu T, Lu W, Li W, Jiang T, Wei S, Yang S, Shen Y.
Ultrasound Obstet Gynecol. 2022 Feb;59(2):226-233. doi: 10.1002/uog.23702.
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation.
Peng C, Chen H, Ren J, Zhou F, Li Y, Keqie Y, Ding T, Ruan J, Wang H, Chen X, Liu S.
BMC Genomics. 2023 Sep 4;24(1):521. doi: 10.1186/s12864-023-09593-x.
Unilateral macrocystic dysplasia and contralateral agenesis in a monoamniotic twin.
Ostatníková Michaela, Doležal Pavel, Gábor Martin, Záhumenský Jozef.
Ceska Gynekol. 2022;87(4):278-281. doi: 10.48095/cccg2022278.
Meckel-Gruber Syndrome with unilateral renal agenesis.
Uysal F, Uysal A.
J Coll Physicians Surg Pak. 2015 Apr;25 Suppl 1:S56-7.
How often do we incidentally find a fetal abnormality at the routine third-trimester growth scan? A population-based study.
Drukker L, Cavallaro A, Salim I, Ioannou C, Impey L, Papageorghiou AT.
Am J Obstet Gynecol. 2020 Dec;223(6):919.e1-919.e13. doi: 10.1016/j.ajog.2020.05.052. Epub 2020 Jun 3.
