Michael B. Petersen

Dual testing with QF‐PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF‐PCR as a stand‐alone test according to referral indications

G. Efstathiou, S. Sifakis, E. Anastasakis, 2012, Prenatal diagnosis.

Prenatal diagnosis of achondroplasia presenting with multiple‐suture synostosis: a novel association

V. Velissariou, T. Antoniadi, C. Karadimas, 2006, Prenatal diagnosis.

Prenatal diagnosis of hypochondroplasia: Report of two cases

S. Sifakis, G. Nasioulas, V. Velissariou, 2006, American journal of medical genetics. Part A.

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

E. Feingold, T. Hassold, G. Karadima, 1997, Human molecular genetics.

Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation‐dependent probe amplification (MLPA) screening

E. Anastasiadou, H. Kontos, S. Orrù, 2008, Prenatal diagnosis.

Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.

E. Blennow, A. Tsezou, G. Karadima, 2000, American journal of medical genetics.