V.K. Maloney

A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis

Sara Benito‐Sanz, N. Simon Thomas, Céline Huber et al. · The American Journal of Human Genetics · 2005 · 133 citations · Full text

Pathogenesis, Histopathology, Pathology +7

15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q

Katrina Tatton‐Brown, Daniela T. Pilz, Karen Helene Ørstavik et al. · American Journal of Medical Genetics Part A · 2009 · 128 citations

Human Growth, Cytogenetics, Genetics +18

Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development

Heather L. Wilson, John A. Crolla, Dena Walker et al. · European Journal of Human Genetics · 2008 · 81 citations · Full text

Developmental Biology, Developmental Cognitive Neuroscience, Developmental Genetics +9

Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect

John Barber, Shuai Zhang, Nicole Friend et al. · Cytogenetic and Genome Research · 2006 · 60 citations

Investigation of the origins of human autosomal inversions

N. Simon Thomas, Victoria Bryant, V.K. Maloney et al. · Human Genetics · 2008 · 30 citations

Developmental Anomaly, Genetics, Human Autosomal Inversions +3