C. de la Iglesia

A New Case with Corpus Callosum Abnormalities, Microcephaly and Seizures Associated with a 2.3-Mb 1q43-q44 Deletion

M. Augé, E. Lloveras, V. Ventura, 2019, Cytogenetic and Genome Research.

Maternal serum alpha‐fetoprotein levels in congenital nephrotic syndrome carrier pregnancies

M. Kestilä, B. Serra, M. Carrera, 1999, Prenatal diagnosis.

Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases

M. Augé, A. Plaja, E. Lloveras, 2021, Cytogenetic and Genome Research.

Early detection of reversed diastolic umbilical flow: should we offer karyotyping?

V. Cusí, M. Torrents, A. Muñoz, 1997, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Identification of two de novo partial trisomies by comparative genomic hybridization

C. Fuster, J. Egozcue, M. Carrera, 2001, Clinical genetics.

Successful Use of a Laser for Human Embryo Biopsy in Preimplantation Genetic Diagnosis: Report of Two Cases

A. Veiga, P. Barri, M. Boada, 1998, Journal of Assisted Reproduction and Genetics.

Quality of recovery following childbirth: a prospective, multicentre cohort study

Richard Smith, V. Sundararajan, D. Uncles, 2023, Anaesthesia.