Literature DB >> 16845280

Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line.

Thomas Liehr.   

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Year:  2006        PMID： 16845280     DOI： 10.1097/00125817-200607000-00011

Source DB:  PubMed          Journal:  Genet Med        ISSN： 1098-3600            Impact factor:   8.822


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  10 in total

1.  Centromere activity in dicentric small supernumerary marker chromosomes.

Authors:  Elisabeth Ewers; Kinya Yoda; Ahmed B Hamid; Anja Weise; Marina Manvelyan; Thomas Liehr
Journal:  Chromosome Res       Date:  2010-06-22       Impact factor: 5.239

Review 2.  Small supernumerary marker chromosomes and uniparental disomy have a story to tell.

Authors:  Thomas Liehr; Elisabeth Ewers; Ahmed B Hamid; Nadezda Kosyakova; Martin Voigt; Anja Weise; Marina Manvelyan
Journal:  J Histochem Cytochem       Date:  2011-06-14       Impact factor: 2.479

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

Authors:  Ruth Mikelsaar; Jelena Lissitsina; Oliver Bartsch
Journal:  J Appl Genet       Date:  2011-04-05       Impact factor: 3.240

Review 4.  Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives.

Authors:  Wafa Slimani; Afef Jelloul; Ahmed Al-Rikabi; Amira Sallem; Yosra Hasni; Salma Chachia; Adel Ernez; Anouar Chaieb; Mohamed Bibi; Thomas Liehr; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Assist Reprod Genet       Date:  2020-05-12       Impact factor: 3.412

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

Authors:  Cui Li; Minggang Zhao; Xiang Wang; Xu Li; Junping Xing
Journal:  Transl Androl Urol       Date:  2021-04

6.  Heteromorphic variants of chromosome 9.

Authors:  Nadezda Kosyakova; Ani Grigorian; Thomas Liehr; Marina Manvelyan; Isabella Simonyan; Hasmik Mkrtchyan; Rouben Aroutiounian; Anna D Polityko; Anna I Kulpanovich; Tatiana Egorova; Evgenia Jaroshevich; Alla Frolova; Natalia Shorokh; Irina V Naumchik; Marianne Volleth; Isolde Schreyer; Heike Nelle; Markus Stumm; Rolf-Dieter Wegner; Gisela Reising-Ackermann; Martina Merkas; Lukretija Brecevic; Thomas Martin; Laura Rodríguez; Samarth Bhatt; Monika Ziegler; Katharina Kreskowski; Anja Weise; Ali Sazci; Svetlana Vorsanova; Marcelo de Bello Cioffi; Emel Ergul
Journal:  Mol Cytogenet       Date:  2013-04-01       Impact factor: 2.009

7.  Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)-Case Report.

Authors:  H C Manju; Supriya Bevinakoppamath; Deepa Bhat; Akila Prashant; Jayaram S Kadandale; P V V Gowri Sairam
Journal:  Mol Cytogenet       Date:  2022-03-26       Impact factor: 2.009

8.  Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them.

Authors:  Thomas Liehr; Kristin Mrasek; Nadezda Kosyakova; Caroline Mackie Ogilvie; Joris Vermeesch; Vladimir Trifonov; Nikolai Rubtsov
Journal:  Mol Cytogenet       Date:  2008-06-04       Impact factor: 2.009

9.  Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.

Authors:  Thomas Liehr; Isolde Schreyer; Alma Kuechler; Emmanouil Manolakos; Sylke Singer; Andreas Dufke; Kathleen Wilhelm; Tereza Jančušková; Radek Čmejla; Moneeb A K Othman; Ahmed H Al-Rikabi; Kristin Mrasek; Monika Ziegler; Stefanie Kankel; Katharina Kreskowski; Anja Weise
Journal:  Mol Cytogenet       Date:  2018-03-09       Impact factor: 2.009

10.  Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the Literature.

Authors:  Thomas Liehr; Anja Weise; Kristin Mrasek; Monika Ziegler; Niklas Padutsch; Kathleen Wilhelm; Ahmed Al-Rikabi
Journal:  Front Genet       Date:  2019-11-14       Impact factor: 4.599
  10 in total

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