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1. Cover Image, Volume 173A, Number 2, February 2017

2. Implication of LRRC4C and DPP6 in neurodevelopmental disorders

5. Clinical features associated with copy number variations of the 14q32 imprinted gene cluster

8. Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients

11. The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

12. Investigation ofNRXN1deletions: Clinical and molecular characterization

16. Referral patterns for microarray testing in prenatal diagnosis

20. Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes

22. The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes

30. Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions

42. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2

43. Neuroimaging findings in children with rare or novel de novo chromosomal anomalies

49. Identification of a novel polymorphism—the duplication of the NPHP1 (nephronophthisis 1) gene

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