Literature DB >> 10051022

Fragile X syndrome: of POF and premutations.

J Macpherson, A Murray, J Webb, P Jacobs.   

Abstract

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Year:  1999        PMID： 10051022      PMCID： PMC1734291     

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

1.  Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors.

Authors:  N McIntosh; L W Gane; A McConkie-Rosell; R L Bennett
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

Review 2.  Transplantation of human umbilical cord mesenchymal stem cells to treat premature ovarian failure.

Authors:  Oldouz Shareghi-Oskoue; Leili Aghebati-Maleki; Mehdi Yousefi
Journal:  Stem Cell Res Ther       Date:  2021-08-11       Impact factor: 8.079

3.  The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter.

Authors:  Daman Kumari; Andrei Gabrielian; David Wheeler; Karen Usdin
Journal:  Biochem J       Date:  2005-03-01       Impact factor: 3.857

4.  Classical fragile-X phenotype in a female infant disclosed by comprehensive genomic studies.

Authors:  Paula Jorge; Elsa Garcia; Ana Gonçalves; Isabel Marques; Nuno Maia; Bárbara Rodrigues; Helena Santos; Jacinta Fonseca; Gabriela Soares; Cecília Correia; Margarida Reis-Lima; Vincenzo Cirigliano; Rosário Santos
Journal:  BMC Med Genet       Date:  2018-05-10       Impact factor: 2.103
  4 in total

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