Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference26 articles.
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2. Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes;Chen;Gene,2013
3. An 18p21q translocation in a patient with presumptive “monosomy G”;Cohen;Am. J. Dis. Child.,1972
4. Early onset of gastric carcinoma and constitutional deletion of 18p;Dellavecchia;Cancer Genet. Cytogenet.,1999
5. Cloning and characterization of cDNA encoding the rabbit tRNA-guanine transglycosylase 60-kilodalton subunit;Deshpande;Arch. Biochem. Biophys.,1996
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2. An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22;NAGOYA J MED SCI;2020
3. Non-invasive prenatal testing detects duplication abnormalities of fetal chromosome 12;European Journal of Obstetrics & Gynecology and Reproductive Biology;2020-10
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