Last Updated: 09/26/2026
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Found 7 publications
Laboratory Stewardship Rescues Misordered Familial Targeted Cytogenetic Testing Following Proband Genomic Testing: Case Series Review.
Journal: Journal of the Association of Genetic Technologists
Published: June 05, 2026
Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion.
Journal: Journal of clinical research in pediatric endocrinology
Published: July 20, 2017
6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy.
Journal: American journal of medical genetics. Part A
Published: March 15, 2016
Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay.
Journal: American journal of medical genetics. Part A
Published: March 20, 2014
Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
Journal: American journal of medical genetics. Part A
Published: February 04, 2013
Clinical comparison of overlapping deletions of 19p13.3.
Journal: American journal of medical genetics. Part A
Published: October 24, 2012
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype.
Journal: American journal of medical genetics. Part A
Published: February 06, 2012
Showing 1-7 of 7
Last Updated: 09/26/2026