Author:
Szczałuba Krzysztof,Jakubiuk-Tomaszuk Anna,Kędzior Marta,Bernaciak Joanna,Zdrodowska Jolanta,Kurzątkowski Wiesław,Radkowski Marek,Demkow Urszula
Publisher
Springer International Publishing
Reference27 articles.
1. Boggula VR, Shukla A, Danda S, Hariharan SV, Nampoothiri S, Kumar R, Phadke SR (2014) Clinical utility of multiplex ligation-dependent probe amplification technique in identification of aetiology of unexplained mental retardation: a study in 203 Indian patients. Indian J Med Res 139:66–75
2. Campos CM, Zanardo EA, Dutra RL, Kulikowski LD, Kim CA (2015) Investigation of copy number variation in children with conotruncal heart defects. Arq Bras Cardiol 104:24–30
3. Crotwell PL, Hoyme HE (2012) Advances in whole-genome genetic testing: from chromosomes to microarrays. Curr Probl Pediatr Adolesc Health Care 42:47–73
4. Gagnon A, Wilson RD, Allen VM, Audibert F, Blight C, Brock JA, Désilets VA, Johnson JA, Langlois S, Murphy-Kaulbeck L, Wyatt P, Society of Obstetricians and Gynaecologists of Canada (2009) Evaluation of prenatally diagnosed structural congenital anomalies. J Obstet Gynaecol Can 31:875–882
5. Geng J, Picker J, Zheng Z, Zhang X, Wang J, Hisama F, Brown DW, Mullen MP, Harris D, Stoler J, Seman A, Miller DT, Fu Q, Roberts AE, Shen Y (2014) Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield. BMC Genomics 15:1127
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