Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report

Abdullah; Cui Li; Minggang Zhao; Xiang Wang; Xu Li; Junping Xing

doi:10.21037/tau-20-1087

Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report

Translational Andrology and Urology ◽

10.21037/tau-20-1087 ◽

2021 ◽

Vol 10 (4) ◽

pp. 1797-1802

Author(s):

Abdullah ◽

Cui Li ◽

Minggang Zhao ◽

Xiang Wang ◽

Xu Li ◽

...

Keyword(s):

Case Report ◽

Hypogonadotropic Hypogonadism ◽

Marker Chromosome ◽

Chromosome 22 ◽

Small Supernumerary Marker Chromosome

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Case Report A small supernumerary marker chromosome, derived from chromosome 22, possibly associated with repeated spontaneous abortions

Genetics and Molecular Research ◽

10.4238/vol9-3gmr947 ◽

2010 ◽

Vol 9 (3) ◽

pp. 1683-1689 ◽

Cited By ~ 5

Author(s):

M. Balkan ◽

H. İsi ◽

A. Gedik ◽

M. Erdemoğlu ◽

T. Budak

Keyword(s):

Case Report ◽

Marker Chromosome ◽

Chromosome 22 ◽

Spontaneous Abortions ◽

Small Supernumerary Marker Chromosome

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Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism

Journal of Applied Genetics ◽

10.1007/s13353-011-0041-5 ◽

2011 ◽

Vol 52 (3) ◽

pp. 331-334 ◽

Cited By ~ 2

Author(s):

Ruth Mikelsaar ◽

Jelena Lissitsina ◽

Oliver Bartsch

Keyword(s):

Hypogonadotropic Hypogonadism ◽

Marker Chromosome ◽

Chromosome 22 ◽

Small Supernumerary Marker Chromosome

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/s1028-4559(10)60081-2 ◽

2010 ◽

Vol 49 (3) ◽

pp. 381-384 ◽

Cited By ~ 7

Author(s):

Chih-Ping Chen ◽

Chyi-Chyang Lin ◽

Yi-Ning Su ◽

Fuu-Jen Tsai ◽

Schu-Rern Chern ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Marker Chromosome ◽

Chromosome 22 ◽

Molecular Cytogenetic ◽

Small Supernumerary Marker Chromosome ◽

Cytogenetic Characterization

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome

Gene ◽

10.1016/j.gene.2013.05.061 ◽

2013 ◽

Vol 527 (1) ◽

pp. 384-388 ◽

Cited By ~ 8

Author(s):

Chih-Ping Chen ◽

Tsang-Ming Ko ◽

Yi-Yung Chen ◽

Jun-Wei Su ◽

Wayseen Wang

Keyword(s):

Prenatal Diagnosis ◽

Marker Chromosome ◽

Chromosome 22 ◽

Molecular Cytogenetic ◽

Small Supernumerary Marker Chromosome ◽

Cat Eye Syndrome ◽

Cytogenetic Characterization

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Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22

International Journal of Pediatrics and Child Health ◽

10.12974/2311-8687.2019.07.5 ◽

2019 ◽

Vol 7 (1) ◽

pp. 36-39

Author(s):

Esra Tug ◽

Keyword(s):

Marker Chromosome ◽

Clinical Spectrum ◽

Chromosome 22 ◽

Small Supernumerary Marker Chromosome

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Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype

Prenatal Diagnosis ◽

10.1002/pd.1520 ◽

2006 ◽

Vol 26 (10) ◽

pp. 898-902 ◽

Cited By ~ 5

Author(s):

Chyi-Chyang Lin ◽

Yao-Yuan Hsieh ◽

Chung-Hsing Wang ◽

Yueh-Chun Li ◽

Lie-Jiau Hsieh ◽

...

Keyword(s):

Marker Chromosome ◽

Chromosome 22 ◽

Normal Phenotype ◽

Small Supernumerary Marker Chromosome ◽

Prenatal Detection

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Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22

Molecular Cytogenetics ◽

10.1186/s13039-016-0248-6 ◽

2016 ◽

Vol 9 (1) ◽

Author(s):

Yu-an Hu ◽

Yingxia Cui ◽

Xiaobo Fan ◽

Qiuyue WU ◽

Weiwei Li ◽

...

Keyword(s):

Genetic Counseling ◽

Prenatal Diagnosis ◽

Angelman Syndrome ◽

Marker Chromosome ◽

Chromosome 22 ◽

Small Supernumerary Marker Chromosome

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A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report

Molecular Cytogenetics ◽

10.1186/1755-8166-2-22 ◽

2009 ◽

Vol 2 (1) ◽

pp. 22 ◽

Cited By ~ 7

Author(s):

Frenny Sheth ◽

Elisabeth Ewers ◽

Nadezda Kosyakova ◽

Anja Weise ◽

Jayesh Sheth ◽

...

Keyword(s):

Case Report ◽

Turner Syndrome ◽

Y Chromosome ◽

Marker Chromosome ◽

Syndrome Patient ◽

Small Supernumerary Marker Chromosome ◽

Turner Syndrome Patient

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Review of "Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22"

Publons reviews and discussion ◽

10.14322/publons.r75500 ◽

2015 ◽

Author(s):

Thomas Liehr

Keyword(s):

Prenatal Diagnosis ◽

Marker Chromosome ◽

Chromosome 22 ◽

Molecular Cytogenetic ◽

Small Supernumerary Marker Chromosome ◽

Cytogenetic Characterization

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Premature ovarian insufficiency associated with a small supernumerary marker chromosome 15: a case report

Endocrine Abstracts ◽

10.1530/endoabs.73.aep609 ◽

2021 ◽

Author(s):

Sawsen Essayeh ◽

Lilia Kraoua ◽

Sabrina Ayari ◽

Zouaoui Chadia ◽

Ridha Mrad ◽

...

Keyword(s):

Case Report ◽

Marker Chromosome ◽

Premature Ovarian Insufficiency ◽

Chromosome 15 ◽

Ovarian Insufficiency ◽

Small Supernumerary Marker Chromosome

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