Search Results - Gullett, Ambrose M.

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  1. 1
    Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux

    Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux by CORDELL, Heather J, DARLAY, Rebecca, KENDA, Rajko B, GOODSHIP, Judith A, CHAROEN, Pimphen, STEWART, Aisling, GULLETT, Ambrose M, LAMBERT, Heather J, MALCOLM, Sue, FEATHER, Sally A, GOODSHIP, Timothy H. J, WOOLF, Adrian S

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  2. 2
    De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure

    De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure by JENKINS, Dagan, BITNER-GLINDZICZ, Maria, SUN, Tung-Tien, WOOLF, Adrian S, MALCOLM, Sue, HU, Chih-Chi A, ALLISON, Jennifer, WINYARD, Paul J. D, GULLETT, Ambrose M, THOMAS, David F. M, BELK, Rachel A, FEATHER, Sally A

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  3. 3
    Primary, Nonsyndromic Vesicoureteric Reflux and Nephropathy in Sibling Pairs: A United Kingdom Cohort for a DNA Bank

    Primary, Nonsyndromic Vesicoureteric Reflux and Nephropathy in Sibling Pairs: A United Kingdom Cohort for a DNA Bank by Lambert, Heather J, Stewart, Aisling, Gullett, Ambrose M, Cordell, Heather J, Malcolm, Sue, Feather, Sally A, Goodship, Judith A, Goodship, Timothy H J, Woolf, Adrian S

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  4. 4
    Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutations

    Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutations by Marks, Stephen D., Gullett, Ambrose M., Brennan, Eileen, Tullus, Kjell, Jaureguiberry, Graciana, Klootwijk, Enriko, Stanescu, Horia C., Kleta, Robert, Woolf, Adrian S.

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