Full Monosomy 21: Echocardiographic Findings in the Third Molecularly Confirmed Case

Author:

Fisher D.,DiPietro A.,Murdison K. A.,Lemieux C. A.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Ghidini A, Fallet S, Robinowitz J, Lockwood CJ, Dische R, Willner J (1993) Prenatal detection of monosomy 21 mosaicism. Prenat Diagn 13:163–169

2. Joosten AM, De VS, Van OD, Brandenburg H, Gaillard JL, Vermeij-Keers C (1997) Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridization. Prenat Diag 17:271–275

3. Mori MA, Lapunzina P, Delicado A, Nunez G, Rodriguez JI et al (2009) A prenatally diagnosed patient with full monosomy 21: ultrasound, cytogenetic, clinical, molecular, and necropsy findings. Am J Med Genet A 127:69–73

4. Nguyen HP, Riess A, Kruger M, Bauer P, Singer S, Schneider M, Enders H, Dufke A (2009) Mosaic trisomy 21/monosomy 21 in a living female infant. Cytogent Genome Res 125:26–32

5. Pellissier MC, Philip N, Voelckel-Baeteman MA, Mattei MG, Mattei JF (1987) Monosomy 21: a new case confirmed by in situ hybridization. Hum Genet 75:95–96

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