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Journal of Zhejiang University. Science. B|January 16, 2008
Genetics in medical school curriculum: a look at the University of Rochester School of Medicine and DentistryDeanne M Robinson, Chin-To Fong
The Clinical Teacher|June 26, 2015
A culinary laboratory for nutrition educationMichael Jacob, Patricia Stewart, Annette Medina-Walpole, et al.
Molecular Cytogenetics|December 21, 2021
MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parentBin Zhang, Michel Liu, Chin-To Fong, et al.
American Journal of Audiology|February 12, 2024
Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or DeafnessAcacia Bowden, Alexandra Hubbel, Lindsay Smith, et al.
Colombia Medica (Cali, Colombia)|January 6, 2021
Applying the functional independence measure to the assessment of patients with mucopolysaccharidosisMarcos Almeida Matos, Paloma Silva Lopes, Allan Rodrigues Corsini, et al.
American Journal of Medical Genetics. Part A|May 13, 2008
Young-Simpson syndrome (YSS), a variant of del(1)(p36) syndrome?Deanne Mraz Robinson, Cecilia C Meagher, Craig C Orlowski, et al.
European Journal of Medical Genetics|December 21, 2012
Deletion 1q43 encompassing only CHRM3 in a patient with autistic disorderAndrea Klunder Petersen, Ausaf Ahmad, Mustafa Shafiq, et al.
Molecular Cytogenetics|February 26, 2021
Diagnosis of FOXG1 syndrome caused by recurrent balanced chromosomal rearrangements: case study and literature reviewConnor P Craig, Emily Calamaro, Chin-To Fong, et al.
Molecular Cytogenetics|October 8, 2021
Allelic and dosage effects of NHS in X-linked cataract and Nance-Horan syndrome: a family study and literature reviewCaroline Miller, Benjamin G Gertsen, Audrey L Schroeder, et al.
American Journal of Medical Genetics. Part A|December 10, 2022
Progressive brain atrophy and severe neurodevelopmental phenotype in siblings with biallelic COASY variantsJustin Rosati, Jessica Johnson, Zinandre Stander, et al.
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