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Prenatal Diagnosis|April 22, 2009
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardiaAngela E Lin, Barbara O'Brien, Laurie A Demmer, et al.
Dermatology Online Journal|May 19, 2024
Milia en plaque on the shoulder as an early manifestations of mycosis fungoidesFelipe Tavares Rodrigues, Gabriela Coutinho Coutinho Chequer Cabral, Priscilla Filippo de Minas Filippo Alvim, et al.
American Journal of Medical Genetics|June 13, 1997
Lateral meningocele syndrome: three new patients and review of the literatureK W Gripp, C I Scott, H E Hughes, et al.
BMC Infectious Diseases|September 7, 2017
Risk factors for increased immune reconstitution in response to Mycobacterium tuberculosis antigens in tuberculosis HIV-infected, antiretroviral-naïve patientsTatiana Pereira da Silva, Carmem Beatriz Wagner Giacoia-Gripp, Carolina A Schmaltz, et al.
Genetics in Medicine Open|December 13, 2024
A novel syndrome associated with prenatal fentanyl exposureErin Wadman, Erica Fernandes, Candace Muss, et al.
Metabolic Brain Disease|November 11, 2021
Moderate-intensity continuous training and high-intensity interval training improve cognition, and BDNF levels of middle-aged overweight menNeumir Sales de Lima, Ricardo Augusto Leoni De Sousa, Fabiano Trigueiro Amorim, et al.
Contemporary Clinical Trials Communications|September 2, 2022
Effects of the association of different volumes of strength training with photobiomodulation therapy on insulin resistance: A protocol for a randomized, triple-blind, placebo-controlled trialPedro Paulo Ribeiro Ferreira, Luís Filipe Rocha Silva, Marco Fabrício Dias-Peixoto, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomaliesMax Krall, Stephanie Htun, Rhonda E Schnur, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
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