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Carole Goumy

Showing results (1-10 of 30) with videos related to

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American Journal of Medical Genetics. Part A|April 4, 2008
Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature reviewPierre Blanc, Laetitia Gouas, Christine Francannet, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 12, 2010
Fetal skin fibroblasts: a cell model for studying the retinoid pathway in congenital diaphragmatic herniaCarole Goumy, Karen Coste, Geoffroy Marceau, et al.
Fetal Diagnosis and Therapy|May 27, 2010
Retinoid pathway and congenital diaphragmatic hernia: hypothesis from the analysis of chromosomal abnormalitiesCarole Goumy, Laetitia Gouas, Geoffroy Marceau, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 3, 2015
Prenatal diagnosis of the VACTERL association using routine ultrasound examinationAnne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, et al.
Plos One|July 7, 2025
Association between shortened maternal and fetal telomere length and abnormal fetal developmentOcéane Coudrieu, Zangbéwendé Guy Ouedraogo, Denis Gallot, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 18, 2013
Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in AuvergneAnne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, et al.
Placenta|August 7, 2025
Shorter umbilical cord telomere length is associated with fetal developmental anomalies and pregnancy lossCarole Goumy, Thérèse Sudy, Océane Coudrieu, et al.
Cancers|April 13, 2023
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute LeukemiaGwendoline Soler, Zangbéwendé Guy Ouedraogo, Carole Goumy, et al.
European Journal of Medical Genetics|July 17, 2012
An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairmentCéline Pebrel-Richard, Stéphan Kemeny, Laetitia Gouas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2010
Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalitiesCarole Goumy, Laetitia Gouas, Céline Pebrel-Richard, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|April 4, 2008
Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature reviewPierre Blanc, Laetitia Gouas, Christine Francannet, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 12, 2010
Fetal skin fibroblasts: a cell model for studying the retinoid pathway in congenital diaphragmatic herniaCarole Goumy, Karen Coste, Geoffroy Marceau, et al.
Fetal Diagnosis and Therapy|May 27, 2010
Retinoid pathway and congenital diaphragmatic hernia: hypothesis from the analysis of chromosomal abnormalitiesCarole Goumy, Laetitia Gouas, Geoffroy Marceau, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 3, 2015
Prenatal diagnosis of the VACTERL association using routine ultrasound examinationAnne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, et al.
Plos One|July 7, 2025
Association between shortened maternal and fetal telomere length and abnormal fetal developmentOcéane Coudrieu, Zangbéwendé Guy Ouedraogo, Denis Gallot, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 18, 2013
Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in AuvergneAnne Debost-Legrand, Carole Goumy, Hélène Laurichesse-Delmas, et al.
Placenta|August 7, 2025
Shorter umbilical cord telomere length is associated with fetal developmental anomalies and pregnancy lossCarole Goumy, Thérèse Sudy, Océane Coudrieu, et al.
Cancers|April 13, 2023
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute LeukemiaGwendoline Soler, Zangbéwendé Guy Ouedraogo, Carole Goumy, et al.
European Journal of Medical Genetics|July 17, 2012
An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairmentCéline Pebrel-Richard, Stéphan Kemeny, Laetitia Gouas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2010
Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalitiesCarole Goumy, Laetitia Gouas, Céline Pebrel-Richard, et al.
Pageof 3