A Rare Case of ins(1)(p22.3q25q32.1) Reported In a Patient With Unbalanced Offspring
Rosemarie Schmidt, MS, CLSp(CG), Stefania Rondinelli, BA, ClSp(CG), Eva Beller, MS,Veena Suri, PhD, Martha Weinstein, PhD,
A rare case of possible 3;1 meiotic segregation and subsequent interchange trisomy 18 in a fetus whose mother carries a t(12;18) (p13.1;q21.1) translocation
Christin M. Coffeen1, Sucheta Bhatt1, Maya Thangavelu1, David B. Rogers1, Lawrence D. Platt2, 3
1Genzyme Genetics, Orange, CA; 2David Geffen School of Medicine at UCLA, Los Angeles, CA; 3Center for Fetal Medicine and Women's Ultrasound, Los Angeles