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Molecular Cytogenetics
|
September 18, 2012
Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies
Isabel Filges, Anjeung Kang, Vanessa Klug, et al.
Prenatal Diagnosis
|
February 26, 2011
aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis
Isabel Filges, Anjeung Kang, Vanessa Klug, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
June 28, 2011
Fetal polydactyly: a study of 24 cases ascertained by prenatal sonography
Isabel Filges, Anjeung Kang, Jürgen Hench, et al.
Swiss Medical Weekly
|
February 28, 2013
First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoa
Christian De Geyter, Oliver Sterthaus, Peter Miny, et al.
BMC Ophthalmology
|
June 3, 2014
Anterior segment dysgenesis associated with Williams-Beuren syndrome: a case report and review of the literature
Margarita G Todorova, Matthias C Grieshaber, Rafael J A Cámara, et al.
Metabolic Engineering
|
April 2, 2013
mRNA transfection-based, feeder-free, induced pluripotent stem cells derived from adipose tissue of a 50-year-old patient
Boon Chin Heng, Karl Heinimann, Peter Miny, et al.
Human Pathology
|
April 22, 2014
Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21
Sylvia Hoeller, Michel P Bihl, Alexandar Tzankov, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome
Isabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
Fertility and Sterility
|
August 27, 2011
A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesis
Isabel Filges, Christophe Kunz, Peter Miny, et al.
Fertility and Sterility
|
February 2, 2010
Parental origin and mechanism of formation of a 46,X,der(X)(pter-->q21.1::p11.4-->pter)/45,X karyotype in a woman with mild Turner syndrome
Franz Binkert, Ana Spreiz, Martina Höckner, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Molecular Cytogenetics
|
September 18, 2012
Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies
Isabel Filges, Anjeung Kang, Vanessa Klug, et al.
Prenatal Diagnosis
|
February 26, 2011
aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis
Isabel Filges, Anjeung Kang, Vanessa Klug, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
June 28, 2011
Fetal polydactyly: a study of 24 cases ascertained by prenatal sonography
Isabel Filges, Anjeung Kang, Jürgen Hench, et al.
Swiss Medical Weekly
|
February 28, 2013
First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoa
Christian De Geyter, Oliver Sterthaus, Peter Miny, et al.
BMC Ophthalmology
|
June 3, 2014
Anterior segment dysgenesis associated with Williams-Beuren syndrome: a case report and review of the literature
Margarita G Todorova, Matthias C Grieshaber, Rafael J A Cámara, et al.
Metabolic Engineering
|
April 2, 2013
mRNA transfection-based, feeder-free, induced pluripotent stem cells derived from adipose tissue of a 50-year-old patient
Boon Chin Heng, Karl Heinimann, Peter Miny, et al.
Human Pathology
|
April 22, 2014
Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21
Sylvia Hoeller, Michel P Bihl, Alexandar Tzankov, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2010
Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome
Isabel Filges, Benno Röthlisberger, Nemya Boesch, et al.
Fertility and Sterility
|
August 27, 2011
A novel missense mutation in the high mobility group domain of SRY drastically reduces its DNA-binding capacity and causes paternally transmitted 46,XY complete gonadal dysgenesis
Isabel Filges, Christophe Kunz, Peter Miny, et al.
Fertility and Sterility
|
February 2, 2010
Parental origin and mechanism of formation of a 46,X,der(X)(pter-->q21.1::p11.4-->pter)/45,X karyotype in a woman with mild Turner syndrome
Franz Binkert, Ana Spreiz, Martina Höckner, et al.
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of 5