Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association

BS Marino, PH Lipkin, JW Newburger, G Peacock… - Circulation, 2012 - Am Heart Assoc
Background—The goal of this statement was to review the available literature on
surveillance, screening, evaluation, and management strategies and put forward a scientific …

[HTML][HTML] Overview of cytogenetic technologies

JU Kang - Korean Journal of Clinical Laboratory Science, 2018 - kjcls.org
Cytogenetic analysis plays an important role in examinations of a variety of human
disorders. Over the years, cytogenetic analysis has evolved to a great extent and become a …

The genomic era of clinical oncology: integrated genomic analysis for precision cancer care

LF Surrey, M Luo, F Chang, MM Li - Cytogenetic and genome research, 2017 - karger.com
Genomic alterations are important biological markers for cancer diagnosis and prognosis,
disease classification, risk stratification, and treatment selection. Chromosomal microarray …

Clinically detectable copy number variations in a Canadian catchment population of schizophrenia

AS Bassett, G Costain, WLA Fung, KJ Russell… - Journal of psychiatric …, 2010 - Elsevier
Copy number variation (CNV) is a highly topical area of research in schizophrenia, but the
clinical relevance is uncertain and the translation to clinical practice is under-studied. There …

Identification of incestuous parental relationships by SNP-based DNA microarrays

CP Schaaf, DA Scott, J Wiszniewska, AL Beaudet - The Lancet, 2011 - thelancet.com
We read the results of the sub-Saharan African medical school study (pub lished online Nov
11, 2010) 1 with interest, but were disappointed that medical student electives were ignored …

Cellomics as integrative omics for cancer

D Boda - Current Proteomics, 2013 - ingentaconnect.com
Omics are wide concepts used to define metadata in life sciences and are increasing in
number with the development of science. Thus the era of omics started with genomics, which …

5q31. 3 Microdeletion syndrome: clinical and molecular characterization of two further cases

N Brown, T Burgess, R Forbes… - American Journal of …, 2013 - Wiley Online Library
ABSTRACT The 5q31. 3 microdeletion syndrome has recently emerged as a distinct clinical
entity, and we report two new patients with de novo deletions of this region, bringing the total …

The hedgehog signal induced modulation of bone morphogenetic protein signaling: an essential signaling relay for urinary tract morphogenesis

R Haraguchi, D Matsumaru, N Nakagata, S Miyagawa… - 2012 - journals.plos.org
Background Congenital diseases of the urinary tract are frequently observed in infants. Such
diseases present a number of developmental anomalies such as hydroureter and …

Clinical phenotype and candidate genes for the 5q31. 3 microdeletion syndrome

K Hosoki, T Ohta, J Natsume, S Imai… - American Journal of …, 2012 - Wiley Online Library
Array‐based technologies have led to the identification of many novel microdeletion and
microduplication syndromes demonstrating multiple congenital anomalies and intellectual …

" Idiopathic" mental retardation and new chromosomal abnormalities

C Galasso, A Lo-Castro, N El-Malhany… - Italian journal of …, 2010 - Springer
Mental retardation is a heterogeneous condition, affecting 1-3% of general population. In the
last few years, several emerging clinical entities have been described, due to the advent of …