E. W. Jabs

Second‐trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findings

E. Jabs, P. Bernstein, S. Gross, 1999, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Reevaluation of the origin of a marker chromosome in a patient with 47,XX,r(13)(p11q34), +mar by molecular cytogenetics

E. Jabs, C. Coss, L. Cooper, 1992, Clinical genetics.

Two different structural abnormalities of chromosome 13 in offspring of chromo‐somally normal parents with two fragile sites

E. Jabs, C. Leonard, E. Mules, 1983, Clinical genetics.