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Julie M. Gastier

Stanford University

5

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654

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Evolutionary relationships among Rel domains indicate functional diversification by recombination

2001 Proceedings of the National Academy of Sciences of the United States of America
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Manifestations and linkage analysis in X‐linked autoimmunity‐immunodeficiency syndrome

2000 American Journal of Medical Genetics
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Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndrome.

2000 Human Mutation
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NOVEL MUTATIONS IN THE WISKOTT-ALDRICH SYNDROME PROTEIN GENE AND THEIR EFFECTS ON TRANSCRIPTIONAL, TRANSLATIONAL, AND CLINICAL PHENOTYPES

1999 Human Mutation
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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

1998 Nature Genetics
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Citations (393)