C. Morales

发表

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis

Y. Shen, M. Obón, A. Soler, 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

MLPA: a prenatal diagnostic tool for the study of congenital heart defects?

Aurora Sánchez, A. Soler, I. Mademont-Soler, 2012, Gene.

Overview of Chromosome Abnormalities in First Trimester Miscarriages: A Series of 1,011 Consecutive Chorionic Villi Sample Karyotypes

Aurora Sánchez, A. Borrell, V. Borobio, 2017, Cytogenetic and Genome Research.

Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion

I. Madrigal, M. Obón, J. Bruguera, 2007, Cytogenetic and Genome Research.

Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion

J. Ballescà, R. Oliva, I. Madrigal, 2008, American journal of medical genetics. Part A.

Relevance of Embryo Aneuploidy in Medically Assisted Reproduction

E. Velilla, C. Morales, 2020 .

Cytogenetic study of spontaneous abortions using semi‐direct analysis of chorionic villi samples detects the broadest spectrum of chromosome abnormalities

Aurora Sánchez, A. Borrell, J. Bruguera, 2008, American journal of medical genetics. Part A.

Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade.

Aurora Sánchez, A. Soler, I. Mademont-Soler, 2011, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation

I. Madrigal, Aurora Sánchez, A. Borrell, 2009, American journal of medical genetics. Part A.

Subtelomeric MLPA: is it really useful in prenatal diagnosis?

I. Madrigal, Aurora Sánchez, J. Bruguera, 2010, Prenatal diagnosis.

Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes.

C. Badenas, M. Milá, A. Nadal, 2009, Fertility and sterility.

Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues.

M. Milá, Aurora Sánchez, V. Catalá, 2010, European journal of medical genetics.

The unresolved origin of uniparental diploid cell lines

Aurora Sánchez, A. Soler, I. Mademont-Soler, 2010 .

Assessment of QF-PCR as the first approach in prenatal diagnosis.

C. Badenas, M. Milá, L. Rodriguez-Revenga, 2010, The Journal of molecular diagnostics : JMD.

A Retrospective and Theoretical Evaluation of Rapid Methods for Detecting Chromosome Abnormalities and Their Implications on Genetic Counseling Based on a Series of 3868 CVS Diagnoses

C. Badenas, M. Milá, L. Rodriguez-Revenga, 2007, Fetal Diagnosis and Therapy.

Duplication/deletion mosaicism of the 7q(21.1 → 31.3) region

I. Madrigal, Aurora Sánchez, A. Soler, 2007, American journal of medical genetics. Part A.

Trisomy of 19.4 Mb region of chromosome 22 and subtelomeric 17p identified in a male without clinical affectation

I. Madrigal, Aurora Sánchez, A. Soler, 2007, American journal of medical genetics. Part A.

Characterization of a 5.8-Mb Interstitial Deletion of Chromosome 3p in a Girl with 46,XX,inv(7)dn Karyotype and Phenotypic Abnormalities

L. Armengol, C. Badenas, M. Milá, 2009, Cytogenetic and Genome Research.

Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability

C. Badenas, Aurora Sánchez, Irene Mademont, 2012, American journal of medical genetics. Part A.

Description of the smallest critical region for Dandy–Walker malformation in chromosome 13 in a girl with a cryptic deletion related to t(6;13)(q23;q32)

L. Armengol, Aurora Sánchez, A. Soler, 2010, American journal of medical genetics. Part A.