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Plos Genetics|March 21, 2009
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome)Esther Meyer, Derek Lim, Shanaz Pasha, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1994
Maternal and fetal brain and plasma levels of cocaine and benzoylecgonine after acute or chronic maternal intravenous administration of cocaineS E Robinson, E K Enters, G F Jackson, et al.
Cancer Research|September 24, 1999
Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancerP Fullwood, S Marchini, J S Rader, et al.
American Journal of Human Genetics|January 9, 2008
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patientsJulie Vogt, Benjamin J Harrison, Hayley Spearman, et al.
Artificial Organs|July 1, 1995
An improved left ventricular cannula for chronic dynamic blood pump supportJ F Antaki, T J Dennis, H Konishi, et al.
Molecular Vision|May 23, 2009
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataractEsther Meyer, Fatimah Rahman, Jessica Owens, et al.
Optics Express|May 3, 2014
Nyquist-shaped dispersion-precompensated subcarrier modulation with direct detection for spectrally-efficient WDM transmissionM S Erkılınç, S Kilmurray, R Maher, et al.
European Journal of Medical Genetics|November 13, 2012
Acrocallosal syndrome: identification of a novel KIF7 mutation and evidence for oligogenic inheritanceDiana M Walsh, Stavit A Shalev, Michael A Simpson, et al.
Genes, Chromosomes & Cancer|August 25, 2020
Pathogenic germline variants in patients with features of hereditary renal cell carcinoma: Evidence for further locus heterogeneityPhilip S Smith, Hannah West, James Whitworth, et al.
Journal of Cardiovascular Electrophysiology|May 8, 2024
P-wave alternans rebound following pulmonary vein isolation predicts atrial arrhythmia recurrenceBruce D Nearing, Guilherme L Fialho, Jonathan W Waks, et al.
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