C. Hernando

Intrachromosomal 3p Insertion as a Cause of Reciprocal Pure Interstitial Deletion and Duplication in Two Siblings: Further Delineation of the Emerging Proximal 3p Deletion Syndrome

M. Del Campo, A. Plaja, E. Lloveras, 2015, Cytogenetic and Genome Research.

Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis

C. Fuster, M. Carrera, R. Baraibar, 2002, Prenatal diagnosis.

Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.

C. Fuster, A. Plaja, E. Sarret, 2004, Fertility and sterility.

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

Philippe M Campeau, Tiziana Granata, Ronnie Wright, 2016, American journal of human genetics.

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

C. Fuster, T. Vendrell, M. M. Pérez, 2002, Journal of medical genetics.

Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region

V. Cirigliano, N. Maiz, A. Plaja, 2016, Cytogenetic and Genome Research.

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

A. Nordgren, B. Kerr, S. Banka, 2016, American journal of human genetics.