Literature DB >> 15811012

Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter.

T Eggermann, D Meschede, H Schüler, S Palm, D Gläser, B Horsthemke, K Eggermann, F Haverkamp, K Zerres.   

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Year:  2005        PMID: 15811012     DOI: 10.1111/j.1399-0004.2005.00427.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  5 in total

1.  X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.

Authors:  Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana B Melo; Isabel M Carreira
Journal:  Mol Cytogenet       Date:  2010-07-20       Impact factor: 2.009

Review 2.  Genomic markers of ovarian reserve.

Authors:  Michelle A Wood; Aleksandar Rajkovic
Journal:  Semin Reprod Med       Date:  2013-10-07       Impact factor: 1.303

3.  Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome.

Authors:  Pooja Chauhan; Sushil Kumar Jaiswal; Anjali Rani Lakhotia; Amit Kumar Rai
Journal:  J Assist Reprod Genet       Date:  2016-07-07       Impact factor: 3.412

4.  Complex X chromosome rearrangement associated with multiorgan autoimmunity.

Authors:  Irén Haltrich; Henriett Pikó; Horolma Pamjav; Anikó Somogyi; Antónia Völgyi; Dezső David; Artúr Beke; Zoltán Garamvölgyi; Eszter Kiss; Veronika Karcagi; György Fekete
Journal:  Mol Cytogenet       Date:  2015-07-19       Impact factor: 2.009

5.  A turner syndrome patient carrying a mosaic distal x chromosome marker.

Authors:  Roberto L P Mazzaschi; Juliet Taylor; Stephen P Robertson; Donald R Love; Alice M George
Journal:  Case Rep Genet       Date:  2014-03-17
  5 in total

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