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Hormone Research in Paediatrics|July 4, 2024
Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre StudyMarco Cappa, Francesco d'Aniello, Maria Cristina Digilio, et al.
Developmental Biology|June 6, 2008
Targeted deletion of Tssk1 and 2 causes male infertility due to haploinsufficiencyBingfang Xu, Zhonglin Hao, Kula N Jha, et al.
Developmental Biology|May 23, 2008
TSKS concentrates in spermatid centrioles during flagellogenesisBingfang Xu, Zhonglin Hao, Kula N Jha, et al.
BMC Medical Genomics|February 13, 2013
Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6Laura Ciocca, Cecilia Surace, Maria Cristina Digilio, et al.
Journal of Insect Physiology|November 20, 2003
Absorption of sugars and amino acids by the epidermis of Aphidius ervi larvaeB Giordana, A Milani, A Grimaldi, et al.
The Annals of Thoracic Surgery|February 21, 2006
Genetic syndromes and outcome after surgical correction of tetralogy of FallotGuido Michielon, Bruno Marino, Roberto Formigari, et al.
Heart Failure Clinics|March 12, 2018
Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathiesGiulio Calcagni, Rachele Adorisio, Simone Martinelli, et al.
Neuropediatrics|February 6, 2025
Congenital Ataxia with Progressive Cerebellar Atrophy, Camptodactyly, and Hypertrichosis: A Novel Recognizable Phenotype for NALCN Heterozygous VariantsJacopo Sartorelli, Lorena Travaglini, Giacomo Garone, et al.
Tropical Medicine & International Health : TM & IH|December 19, 2015
Comparison of immune responses to a killed bivalent whole cell oral cholera vaccine between endemic and less endemic settingsSachin N Desai, Zenebe Akalu, Mekonnen Teferi, et al.
European Journal of Medical Genetics|September 7, 2018
TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerationsMarcello Niceta, Sabina Barresi, Francesca Pantaleoni, et al.
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