An interstitial deletion of 8q23.3–q24.22 associated with Langer–Giedion syndrome, Cornelia de Lange syndrome and epilepsy
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
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2. Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome;Cytogenetic and Genome Research;2022
3. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound;Taiwanese Journal of Obstetrics and Gynecology;2017-12
4. Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion;Molecular Cytogenetics;2015-12
5. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3–q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1;Taiwanese Journal of Obstetrics and Gynecology;2015-10
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