Balanced Robertsonian translocation mosaicism of mosaic 45,XY,der(13;21) (q10;q10)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no perinatal decrease of the cell line with the balanced Robertsonian translocation

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Main Author:	Chih-Ping Chen (Author)
Format:	Book
Published:	Elsevier, 2024-07-01T00:00:00Z.
Subjects:	article
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Mosaicism for Robertsonian jumping translocation at amniocentesis: 45,XY,der(15;22)(q10;q10)mat/46,XY,i(15)(q10)/46,XY, genetic counseling, prenatal diagnosis and postnatal follow-up in a pregnancy with a favorable fetal outcome
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Published: (2023)

Balanced reciprocal translocation mosaicism of mosaic 46,XY,t(4;10) (q12;p12.32)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the balanced translocation cell line
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Various endocrine disorders in children with t(13;14)(q10;q10) Robertsonian translocation
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Mosaic 46,XY,der(15)t(6;15)(q25.1;p12)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and postnatal decrease of the aneuploid cell line with the unbalanced translocation
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Mosaic 46,XY,dup(14) (q12q22.3)/46, XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues
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Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcome
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Mosaic distal 13q duplication due to mosaic unbalanced translocation of 46,XY,der(14)t(13;14)(q32.2;p13)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
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Rapid diagnosis of maternal origin of de novo fetal Robertsonian translocation down syndrome of 46,XY,der(13;21)(q10;q10),+21 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with increased nuchal translucency and an abnormal result of first-trimester maternal serum screening
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Mosaic distal 10q deletion or 46,XY,del(10) (q26.13)/46,XY at amniocentesis and cordocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
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Published: (2024)

Low-level mosaic trisomy 21 due to mosaic unbalanced Robertsonian translocation of 46,XX,+21,der(21;21) (q10;q10)/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, cytogenetic discrepancy among various tissues and perinatal progressive decrease of the trisomy 21 cell line
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Mosaicism for r(20) or 46,XY,r(20)(p13q13.3)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the r(20) cell line with no genomic imbalance
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Published: (2024)

Detection of mosaicism for 46,X,i(Y) (q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46, XY at amniocentesis and cytogenetic discrepancy in various tissues
by: Chih-Ping Chen, et al.
Published: (2022)

High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues
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Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report
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Published: (2021)

Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
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Mosaic Turner Syndrome Presenting with a 46,XY Karyotype
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Acne in Klinefelter syndrome-46XY/47XXY mosaicism?
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Genetic counseling of mosaicism for balanced or unbalanced translocation with a normal cell line at amniocentesis
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Incidental detection of familial 8p23.2 microduplication encompassing CSMD1 associated with mosaic 46,XY,t(7;8)(q31.2;p23.1)/46,XY at amniocentesis in a pregnancy with no apparent phenotypic abnormality and a favorable outcome
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Published: (2024)

Mosaicism for 47,XXY or 47,XXY/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the 47,XXY cell line
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Down Syndrome Resulting from a Rare non-Robertsonian Translocation t(11;21)(p13;q22)
by: Dante Bruno Avanso Rosan, et al.
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Preimplantation genetic diagnosis by fluorescence in situ hybridization of reciprocal and Robertsonian translocations
by: Chun-Kai Chen, et al.
Published: (2014)

Clinical and hormonal characteristics and growth data of 45,X/46,XY mosaicism in 38 Chinese patients
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Published: (2023)

Growth data and tumour risk of 32 Chinese children and adolescents with 45,X/46,XY mosaicism
by: Lili Pan, et al.
Published: (2019)

Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)
by: Chih-Ping Chen, et al.
Published: (2022)

Detection of mosaic ring chromosome 12 or 46,XY,r(12) (p13.3q24.33)/46, XY in a 37-year-old male associated with oligospermia but no other apparently phenotypic abnormalities
by: Chih-Ping Chen
Published: (2024)

The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers
by: Shuo Zhang, et al.
Published: (2017)

Balanced Reciprocal Translocations Detected at Amniocentesis
by: Chih-Ping Chen, et al.
Published: (2010)

Assisted Reproductive Treatment Applications in Men With Normal Phenotype But 45,X/46,Xy Mosaic Karyotype: Clinical and Genetic Perspectives
by: Sevtap Kilic, et al.
Published: (2010)

Mosaic 45,X/46, XX at amniocentesis with high-level mosaicism for 45,X in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell line
by: Chih-Ping Chen, et al.
Published: (2023)

The robertsonian translocation of '21/22' in nonobstructive azoospermia: A rare case report from India
by: Paresh Singhal, et al.
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"Not all De novo Robertsonian translocations are truly De novo" - A thought-provoking perspective
by: Dolat Singh Shekhawat, et al.
Published: (2024)

High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line
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Published: (2022)

An Infertile Man with Complementary Isochromosome of 46, XY, I(5)(P10),I(5)(Q10): A Case Report
by: Yu HE, et al.
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Premature Ovarian Failure in a Patient with Robertsonian Translocation Rob (14;15): Is it only a Coincidence?
by: Sebnem Alanya Tosun, et al.
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Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome
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Published: (2021)

A prenatal case misunderstood as specimen confusion: 46,XY/46,XY chimerism
by: Lin Chen, et al.
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Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report
by: Jing SHA, et al.
Published: (2017)

High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell line
by: Chih-Ping Chen
Published: (2024)

Low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell line
by: Chih-Ping Chen
Published: (2024)

Balanced Robertsonian translocation mosaicism of mosaic 45,XY,der(13;21) (q10;q10)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no perinatal decrease of the cell line with the balanced Robertsonian translocation

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