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American Journal of Medical Genetics. Part A
|
August 5, 2010
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)
Irene Mademont-Soler, Carme Morales, Lluís Armengol, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
April 16, 2011
Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade
Irene Mademont-Soler, Carme Morales, Núria Clusellas, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Further defining the critical genes for the 4q21 microdeletion disorder
Xuyun Hu, Xiaoli Chen, Bingbing Wu, et al.
Cytogenetic and Genome Research
|
June 30, 2017
Overview of Chromosome Abnormalities in First Trimester Miscarriages: A Series of 1,011 Consecutive Chorionic Villi Sample Karyotypes
Anna Soler, Carme Morales, Irene Mademont-Soler, et al.
Prenatal Diagnosis
|
October 12, 2010
Subtelomeric MLPA: is it really useful in prenatal diagnosis?
Irene Mademont-Soler, Carme Morales, Jordi Bruguera, et al.
Prenatal Diagnosis
|
April 26, 2024
Novel variant in ACTA1 identified in a fetus with akinesia deformation sequence and cortical development delay
Clara Martínez-Diago, Irene Mademont-Soler, Alexandra Bonmatí, et al.
Gene
|
March 27, 2012
MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
Irene Mademont-Soler, Carme Morales, Anna Soler, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2009
Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation
Irene Mademont-Soler, Carme Morales, Irene Madrigal, et al.
European Journal of Medical Genetics
|
March 31, 2010
Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues
Carme Morales, Esther Cuatrecasas, Irene Mademont-Soler, et al.
Fertility and Sterility
|
May 16, 2009
Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes
Carme Morales, Anna Soler, Cèlia Badenas, et al.
Page
of 3
Search research articles
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Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics. Part A
|
August 5, 2010
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)
Irene Mademont-Soler, Carme Morales, Lluís Armengol, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
April 16, 2011
Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade
Irene Mademont-Soler, Carme Morales, Núria Clusellas, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Further defining the critical genes for the 4q21 microdeletion disorder
Xuyun Hu, Xiaoli Chen, Bingbing Wu, et al.
Cytogenetic and Genome Research
|
June 30, 2017
Overview of Chromosome Abnormalities in First Trimester Miscarriages: A Series of 1,011 Consecutive Chorionic Villi Sample Karyotypes
Anna Soler, Carme Morales, Irene Mademont-Soler, et al.
Prenatal Diagnosis
|
October 12, 2010
Subtelomeric MLPA: is it really useful in prenatal diagnosis?
Irene Mademont-Soler, Carme Morales, Jordi Bruguera, et al.
Prenatal Diagnosis
|
April 26, 2024
Novel variant in ACTA1 identified in a fetus with akinesia deformation sequence and cortical development delay
Clara Martínez-Diago, Irene Mademont-Soler, Alexandra Bonmatí, et al.
Gene
|
March 27, 2012
MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
Irene Mademont-Soler, Carme Morales, Anna Soler, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2009
Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation
Irene Mademont-Soler, Carme Morales, Irene Madrigal, et al.
European Journal of Medical Genetics
|
March 31, 2010
Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues
Carme Morales, Esther Cuatrecasas, Irene Mademont-Soler, et al.
Fertility and Sterility
|
May 16, 2009
Reproductive consequences of genome-wide paternal uniparental disomy mosaicism: description of two cases with different mechanisms of origin and pregnancy outcomes
Carme Morales, Anna Soler, Cèlia Badenas, et al.
Page
of 3