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Cancer Treatment and Research Communications|February 7, 2021
EGFR mutation testing and TKI treatment patterns among veterans with stage III and IV non-small cell lung cancerAnna Hung, Kyung Min Lee, Patrick R Alba, et al.
European Journal of Medical Genetics|July 22, 2018
NRXN1 deletion syndrome; phenotypic and penetrance data from 34 familiesMaryam Al Shehhi, Eva B Forman, Jacqueline E Fitzgerald, et al.
Child Abuse & Neglect|May 7, 2018
Comparing disciplinary methods used by mothers in Palestine and QatarMadeeha Kamal, Samia Halileh, Soha Dargham, et al.
American Journal of Respiratory and Critical Care Medicine|October 22, 2016
Idiopathic Pulmonary Fibrosis: The Association between the Adaptive Multiple Features Method and Fibrosis OutcomesMargaret L Salisbury, David A Lynch, Edwin J R van Beek, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
American Journal of Epidemiology|May 9, 2023
Heterogeneity and Progression of Chronic Obstructive Pulmonary Disease: Emphysema-Predominant and Non-Emphysema-Predominant DiseasePeter J Castaldi, Zhonghui Xu, Kendra A Young, et al.
Hepatology Communications|July 5, 2024
Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver diseaseDavid E Kaplan, Craig C Teerlink, Tae-Hwi Schwantes-An, et al.
Arthritis Care & Research|May 28, 2010
Association between patella alta and the prevalence and worsening of structural features of patellofemoral joint osteoarthritis: the multicenter osteoarthritis studyJ J Stefanik, Y Zhu, A C Zumwalt, et al.
Clinical Dysmorphology|July 29, 2016
Rubinstein-Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrumMark J Hamilton, Ruth Newbury-Ecob, Muriel Holder-Espinasse, et al.
Nature Genetics|February 2, 2000
A role for smad6 in development and homeostasis of the cardiovascular systemK M Galvin, M J Donovan, C A Lynch, et al.
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