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Poisonous plants: An ongoing problem

Anales de pediatría (Barcelona, Spain : 2003), 2015-05, Vol.82 (5), p.347-353

2015

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Prenatal diagnosis of abdominal mass: review of the foetus in foetu

Anales de pediatría (Barcelona, Spain : 2003), 2015-02, Vol.82 (2), p.101

2015

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

Cytogenetic and genome research, 2017, Vol.152 (2), p.81-89

2017

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

Ultrasound in obstetrics & gynecology, 2013-04, Vol.41 (4), p.375-382

2013

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Case report: Challenges in immune reconstitution following hematopoietic stem cell transplantation for CTLA-4 insufficiency-like primary immune regulatory disorders

Frontiers in immunology, 2022-12, Vol.13, p.1070068

2022

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

American journal of medical genetics. Part A, 2008-01, Vol.146A (1), p.66-70

2008

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Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency

Journal of clinical immunology, 2021, Vol.41 (1), p.171-184

2021

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A 92,XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy

Cytogenetic and genome research, 2016-01, Vol.149 (4), p.258-261

2016

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

Gene, 2012-05, Vol.500 (1), p.151-154

2012

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Subtelomeric MLPA: is it really useful in prenatal diagnosis?

Prenatal diagnosis, 2010-12, Vol.30 (12-13), p.1165-1169

2010

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Epidemiological characteristics in suicidal adolescents seen in the Emergency Department

Anales de pediatría (Barcelona, Spain : 2003), 2016-07, Vol.85 (1), p.13

2016

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

American journal of medical genetics. Part A, 2012-03, Vol.158A (3), p.611-616

2012

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

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2820-2823

2009

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

Cytogenetic and genome research, 2007-04, Vol.116 (4), p.319-323

2007

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

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1335-1340

2008

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Postnatal cytogenetic diagnosis in Spain: analysis, evolution and outcome evaluation over a decade

Medicina clínica, 2007-11, Vol.129 (17), p.664-668

2007

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Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14′, 15, and 21 leading to balanced and unbalanced rearrangements in offspring

American journal of medical genetics. Part A, 2005-04, Vol.134A (3), p.309-314

2005

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

American journal of medical genetics. Part A, 2007-10, Vol.143A (20), p.2423-2429

2007

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Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements

Journal of medical genetics, 1999-04, Vol.36 (4), p.333-334

1999

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Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis

Journal of medical genetics, 1998-09, Vol.35 (9), p.727-730

1998

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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

Fetal diagnosis and therapy, 2008-02, Vol.23 (2), p.126-131

2008

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

American journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.179-183

2007

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SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite

American journal of medical genetics, 2000-01, Vol.90 (1), p.25-28

2000

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Comparative Study of Sequential Combinations of Paclitaxel and Methotrexate on a Human Bladder Cancer Cell Line

Cancer investigation, 2000, Vol.18 (5), p.429-435

2000

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Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSF) as a mitogen of immature cells in fetal blood cultures

Prenatal diagnosis, 1999-01, Vol.19 (1), p.17-20

1999

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Poisonous plants: An ongoing problem

Prenatal diagnosis of abdominal mass: review of the foetus in foetu

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

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

Case report: Challenges in immune reconstitution following hematopoietic stem cell transplantation for CTLA-4 insufficiency-like primary immune regulatory disorders

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

Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary Immunodeficiency

A 92,XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy

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

Subtelomeric MLPA: is it really useful in prenatal diagnosis?

Epidemiological characteristics in suicidal adolescents seen in the Emergency Department

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

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

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

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

Postnatal cytogenetic diagnosis in Spain: analysis, evolution and outcome evaluation over a decade

Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14′, 15, and 21 leading to balanced and unbalanced rearrangements in offspring

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

Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis

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

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

SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite

Comparative Study of Sequential Combinations of Paclitaxel and Methotrexate on a Human Bladder Cancer Cell Line

Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSF) as a mitogen of immature cells in fetal blood cultures

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