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Refinado por: assunto: Cytogenetics remover Nome da Publicação: Molecular Cytogenetics remover
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Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome
Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome
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Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome

He, Si ; Xi, Hui ; Chen, Jing ; Wang, Dan ; Pang, Jialun ; Hu, Jiancheng ; Liu, Qin ; Jia, Zhengjun ; Wang, Hua

Molecular cytogenetics, 2020-02, Vol.13 (1), p.7-7, Article 7 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family
Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family
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Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family

Tang, Wenjuan ; Chen, Guowei ; Xia, Jingshu ; Zhang, Ying

Molecular cytogenetics, 2022-07, Vol.15 (1), p.1-28, Article 28 [Periódico revisado por pares]

London: BioMed Central Ltd

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3
Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
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Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis

Yang, Yang ; Hao, Wang

Molecular cytogenetics, 2023-09, Vol.16 (1), p.1-23, Article 23 [Periódico revisado por pares]

London: BioMed Central Ltd

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4
Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study
Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study
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Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study

Yang, Zhihong ; Liu, Jiaen ; Collins, Gary S ; Salem, Shala A ; Liu, Xiaohong ; Lyle, Sarah S ; Peck, Alison C ; Sills, E Scott ; Salem, Rifaat D

Molecular cytogenetics, 2012-05, Vol.5 (1), p.24-24, Article 24 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies
Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies
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Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies

Tan, Ya-Qi ; Tan, Yue-Qiu ; Cheng, De-Hua

Molecular cytogenetics, 2020-05, Vol.13 (1), p.15-6, Article 15 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array
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Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array

Zhang, Pingping ; Sun, Yanmei ; Huo, Ping ; Tian, Haishen ; Gao, Jian ; Li, Yali

Molecular cytogenetics, 2020-04, Vol.13 (1), p.12-6, Article 12 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Molecular cytogenetic analysis of early spontaneous abortions conceived from varying assisted reproductive technology procedures
Molecular cytogenetic analysis of early spontaneous abortions conceived from varying assisted reproductive technology procedures
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Molecular cytogenetic analysis of early spontaneous abortions conceived from varying assisted reproductive technology procedures

Wu, Tonghua ; Yin, Biao ; Zhu, Yuanchang ; Li, Guangui ; Ye, Lijun ; Chen, Chunmei ; Zeng, Yong ; Liang, Desheng

Molecular cytogenetics, 2016-10, Vol.9 (1), p.79-79, Article 79 [Periódico revisado por pares]

England: BioMed Central Ltd

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8
Cytogenetic contribution to uniparental disomy (UPD)
Cytogenetic contribution to uniparental disomy (UPD)
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Cytogenetic contribution to uniparental disomy (UPD)

Liehr, Thomas

Molecular cytogenetics, 2010-03, Vol.3 (1), p.8-8 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Clinical, cytogenetic, and molecular findings of isodicentric Y chromosomes
Clinical, cytogenetic, and molecular findings of isodicentric Y chromosomes
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Clinical, cytogenetic, and molecular findings of isodicentric Y chromosomes

Yang, Yang ; Hao, Wang

Molecular cytogenetics, 2019-12, Vol.12 (1), p.55-55, Article 55 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature
Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature
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Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature

Marchina, Eleonora ; Forti, Michela ; Tonelli, Mariella ; Maccarini, Stefania ; Malvestiti, Francesca ; Piantoni, Chiara ; Filippini, Elena ; Fazzi, Elisa ; Borsani, Giuseppe

Molecular cytogenetics, 2021-01, Vol.14 (1), p.6-6, Article 6 [Periódico revisado por pares]

England: BioMed Central Ltd

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