K Lillquist

Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation

Matthew A. Deardorff, Maninder Kaur, Dinah Yaeger et al. · The American Journal of Human Genetics · 2007 · 518 citations · Full text

Developmental Anomaly, Smc1a Cause, Mendelian Disorder +11

Further delineation of the 22q13 deletion syndrome

Suzanne Granhøj Lindquist, M. Kirchhoff, Claes Lundsteen et al. · Clinical Dysmorphology · 2005 · 47 citations

Down Syndrome, Karyotype Imaging, Dna Markers +15

THE ABSENCE OF FACTOR II IN A CHILD WITH SYSTEMIC LUPUS ERYTHEMATOSUS

K Lillquist, J. Dyerberg, Morten Krogh-Jensen · Acta Paediatrica · 1978 · 25 citations

PRIMARY HYPERPARATHYROIDISM IN INFANCY ASSOCIATED WITH FAMILIAL HYPOCALCIURIC HYPERCALCEMIA

K Lillquist, Niels Ove Illum, Bendt Brock Jacobsen et al. · Acta Paediatrica · 1983 · 23 citations

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism associated with mutations in the human Ca²+-sensing receptor gene in three Danish families

Peter Schwarz, Nadja Larsen, I. M. Lønborg Friis et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 2000 · 21 citations