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Molecular cytogenetics

Showing results (1-10 of 1,030) with videos related to

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Molecular Cytogenetics|June 27, 2022
First case of two supernumerary markers derived from chromosome 5 and chromosome 8Roberta Giansante, Chiara Palka Bayard De Volo, Melissa Alfonsi, et al.
Molecular Cytogenetics|July 5, 2022
Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese familyWenjuan Tang, Guowei Chen, Jingshu Xia, et al.
Molecular Cytogenetics|March 27, 2020
Copy number variations associated with fetal congenital kidney malformationsMeiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics|August 29, 2020
Prenatal diagnosis of mosaic trisomy 2 and literature reviewTing Wang, Jufei Lian, Congmian Ren, et al.
Molecular Cytogenetics|July 9, 2021
A Turner syndrome case associated with dic(Y;22)Rie Kawamura, Hidehito Inagaki, Midori Yamada, et al.
Molecular Cytogenetics|December 18, 2020
Confined placental mosaicism of Duchenne muscular dystrophy: a case reportMax Winerdal, Eini Westenius, Michaela Granfors, et al.
Molecular Cytogenetics|December 21, 2022
Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 geneMan Luo, Xia Gu, Ting Zhou, et al.
Molecular Cytogenetics|June 6, 2022
Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotypeJieping Song, Wei Jiang, Chengcheng Zhang, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Molecular Cytogenetics|October 6, 2010
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girlWalid Al Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Pageof 103

Showing results (1-10 of 1,030) with videos related to

Sort By:
Pageof 103
Molecular Cytogenetics|June 27, 2022
First case of two supernumerary markers derived from chromosome 5 and chromosome 8Roberta Giansante, Chiara Palka Bayard De Volo, Melissa Alfonsi, et al.
Molecular Cytogenetics|July 5, 2022
Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese familyWenjuan Tang, Guowei Chen, Jingshu Xia, et al.
Molecular Cytogenetics|March 27, 2020
Copy number variations associated with fetal congenital kidney malformationsMeiying Cai, Na Lin, Linjuan Su, et al.
Molecular Cytogenetics|August 29, 2020
Prenatal diagnosis of mosaic trisomy 2 and literature reviewTing Wang, Jufei Lian, Congmian Ren, et al.
Molecular Cytogenetics|July 9, 2021
A Turner syndrome case associated with dic(Y;22)Rie Kawamura, Hidehito Inagaki, Midori Yamada, et al.
Molecular Cytogenetics|December 18, 2020
Confined placental mosaicism of Duchenne muscular dystrophy: a case reportMax Winerdal, Eini Westenius, Michaela Granfors, et al.
Molecular Cytogenetics|December 21, 2022
Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 geneMan Luo, Xia Gu, Ting Zhou, et al.
Molecular Cytogenetics|June 6, 2022
Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotypeJieping Song, Wei Jiang, Chengcheng Zhang, et al.
Molecular Cytogenetics|September 7, 2010
Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportChristel Eckmann-Scholz, Stefan Gesk, Inga Nagel, et al.
Molecular Cytogenetics|October 6, 2010
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girlWalid Al Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Pageof 103