subject area of
- 15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients Academic Article
- A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder Academic Article
- Acute Lymphoblastic Leukemia in a Patient With Constitutional Chromosome 1pter-p36.31 Duplication and 1q43-qter Deletion Academic Article
- Amplification of the prolactin receptor gene in mammary lobular neoplasia Academic Article
- Array-based Comparative Genomic Hybridization (aCGH) Analysis is a Useful Tool for Distinguishing Primary Pulmonary From Metastatic Neuroendocrine Carcinoma to the Lung Academic Article
- Balanced translocation t(3;18)(p13;q22.3) and points mutation in the ZNF407 gene detected in patients with both moderate non-syndromic intellectual disability and autism Academic Article
- Characterization of human embryonic stem cells with features of neoplastic progression Academic Article
- Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 Academic Article
- Comparative Genome Analysis Provides Insights into the Evolution and Adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum Academic Article
- Duplication ofAKT3as a cause of macrocephaly in duplication 1q43q44 Academic Article
- Eosinophilic, Solid, and Cystic Renal Cell Carcinoma Academic Article
- Low‐depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution Academic Article
- MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis Academic Article
- Partial monosomy 1q43 and partial trisomy 20q13.2: a case report Academic Article
- Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results Academic Article
- Polar body array CGH for prediction of the status of the corresponding oocyte. Part II: technical aspects Academic Article
- QF-PCR rapid aneuploidy screen and aCGH analysis of cell free fetal (cff) DNA in supernatant of compromised amniotic fluids (AF) Academic Article
- RETIRED: Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada Academic Article
- Rainbow trout exposed to benzo[a]pyrene yields conserved microRNA binding sites in DNA methyltransferases across 500 million years of evolution Academic Article
- Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder Academic Article
- Severe intellectual disability and autistic features associated with microduplication 2q23.1 Academic Article