Literature DB >> 22887749

A case of de Barsy syndrome with a severe eye phenotype.

Mohammed Al-Owain1, Shamsa Alanazi, Ola Khalifa, Amal Al-Hemidan, Loai Al-Ebdi, Bandar Al-Saud, Fowzan S Alkuraya.   

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Year:  2012        PMID： 22887749     DOI： 10.1002/ajmg.a.35507

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  1 in total

1.  Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue.

Authors:  Anas M Alazami; Sarah M Al-Qattan; Eissa Faqeih; Amal Alhashem; Muneera Alshammari; Fatema Alzahrani; Mohammed S Al-Dosari; Nisha Patel; Afaf Alsagheir; Bassam Binabbas; Hamad Alzaidan; Abdulmonem Alsiddiky; Nasser Alharbi; Majid Alfadhel; Amal Kentab; Riza M Daza; Martin Kircher; Jay Shendure; Mais Hashem; Saif Alshahrani; Zuhair Rahbeeni; Ola Khalifa; Ranad Shaheen; Fowzan S Alkuraya
Journal:  Hum Genet       Date:  2016-03-29       Impact factor: 4.132
  1 in total

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