Ring Chromosome 6
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-47530-6_10
Reference33 articles.
1. Ahzad HA, Ramli SF, Loong TM, Salahshourifar I, Zilfalil BA, Yusoff NM (2010) De novo ring chromosome 6 in a child with multiple congenital anomalies. Kobe J Med Sci 56(2):E79–84
2. Andrieux J, Devisme L, Valat A-S, Robert Y, Frnka C, Savary JB (2005) Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: Case report and review of the literature. Europ J Med Genet 48(2):199–206. https://doi.org/10.1016/j.ejmg.2005.01.028
3. Bieller A, Pasche B, Frank S, Gläser B, Kunz J, Witt K, Zoll B (2001) Isolation and characterization of the human forkhead gene FOXQ1. DNA Cell Biol 20(9):555–561. https://doi.org/10.1089/104454901317094963
4. Birnbacher R, Chudoba I, Pirc-Danoewinata H, König M, Kohlhauser C, Schnedl W, Haas OA (2001) Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome. Ann Génét 44(1):13–18. https://doi.org/10.1016/S0003-3995(00)01033-9
5. Carnevale A, Blanco B, Castillo J, del Castillo V, Dominguez D (1979) Ring chromosome 6 in a child with minimal abnormalities. Am J Med Genet 4(3):271–277. https://doi.org/10.1002/ajmg.1320040310
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