Literature DB >> 2231657

Deletion Xp22.3.

I K Temple, N R Dennis.   

Abstract

Mesh：

Year:  1990        PMID： 2231657      PMCID： PMC1017228          DOI： 10.1136/jmg.27.9.598

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


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  2 in total

1.  De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.

Authors:  I K Temple; J A Hurst; S Hing; L Butler; M Baraitser
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318

2.  Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

Authors:  L I al-Gazali; R F Mueller; A Caine; A Antoniou; A McCartney; M Fitchett; N R Dennis
Journal:  J Med Genet       Date:  1990-01       Impact factor: 6.318
  2 in total

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