References
- Vogel W, Siebers JW, Reinwein H. Partial trisomy 7q. Ann Genet 1973;16:277-80
- Speleman F, Callens B, Logghe K, Van Roy N, Horsley SW, Jauch A, et al. Subtelomeric familial translocation t(2;7)(q37; q35) leading to partial trisomy 7q35→qter: molecular cytogenetic analysis and clinical phenotype in two generations. Am J Med Genet 2000;93:349-54 https://doi.org/10.1002/1096-8628(20000828)93:5<349::AID-AJMG2>3.0.CO;2-S
- Rodríguez L, López F, Paisán L, de la Red Mdel M, Ruiz AM, Blanco M, et al. Pure partial trisomy 7q: two new patients and review. Am J Med Genet 2002;113:218-24 https://doi.org/10.1002/ajmg.10719
- Forabosco A, Baroncini A, Dalpra L, Chessa L, Giannotti A, Maccagnani F, et al. The phenotype of partial dup(7q) reconsidered: a report of five new cases. Clin Genet 1988;34:48-59 https://doi.org/10.1111/j.1399-0004.1988.tb02615.x
- Courtens W, Vroman S, Vandenhove J, Wiedemann U, Schinzel A. Pre-and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7). Prenat Diagn 2001;21:642-8 https://doi.org/10.1002/pd.30
- Vermeesch JR, Thoelen R, Salden I, Raes M, Matthijs G, Fryns JP. Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event. J Med Genet 2003;40:e93 https://doi.org/10.1136/jmg.40.8.e93
- Reddy KS. A paternally inherited terminal deletion, del(8) (p23.1)pat, detected prenatally in an amniotic fluid sample: a review of deletion 8p23.1 cases. Prenat Diagn 1999;19:868-72 https://doi.org/10.1002/(SICI)1097-0223(199909)19:9<868::AID-PD641>3.0.CO;2-A
- Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, et al. Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects. Circulation 2000;10:432-7
- Devriendt K, Matthijs G, Van Dael R, Gewillig M, Eyskens B, Hjalgrim H, et al. Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. Am J Hum Genet 1999;64:1119-26 https://doi.org/10.1086/302330
- Shimokawa O, Miyake N, Yoshimura T, Sosonkina N, Harada N, Mizuguchi T, et al. Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia. Am J Med Genet A 2005;136:49-51