Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb02382.x/fullpdf
Reference28 articles.
1. Terminal deletion of the long arm of chromosome 7: five new cases;Bogart;Am J Med Genet,1990
2. Case of cyclopia with an unbalanced karyotype attributable to a balanced 3/7 translocation;Burrig;Clin Genet,1989
3. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity;Corsello;Am J Med Genet,1990
4. Report of the committee on clinical disorders, chromosome aberrations, and uniparental disomy;Frézal;Cytogenet Cell Genet,1991
5. A girl with karyotype 46, XX, del(7)(pter-q32:);Friedrich;Hum Genet,1979
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1. Holoprosencephaly;Atlas of Genetic Diagnosis and Counseling;2017
2. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature;Taiwanese Journal of Obstetrics and Gynecology;2015-06
3. Holoprosencephaly;Atlas of Genetic Diagnosis and Counseling;2015
4. Holoprosencephaly;Atlas of Genetic Diagnosis and Counseling;2012
5. Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy;Taiwanese Journal of Obstetrics and Gynecology;2011-12
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