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M A Patton

Showing results (71-80 of 110) with videos related to

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Clinical Dysmorphology|October 25, 2000
Further delineation of the DOOR syndromeA Rajab, A Riaz, G Paul, et al.
Journal of Medical Genetics|March 1, 1991
Floating-Harbor syndromeM A Patton, J Hurst, D Donnai, et al.
Clinical Genetics|March 3, 2009
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasiaM A Simpson, A Scheuerle, J Hurst, et al.
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.
Developmental Medicine and Child Neurology|February 1, 1997
Agenesis of the corpus callosum in Turner syndrome with ring XS E Abd, L Wilson, P Howlin, et al.
Genetic Testing|February 24, 2001
Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversionA R Afzal, R N Florêncio, R Taylor, et al.
Journal of Medical Genetics|May 1, 1990
Restrictive dermopathy: a report of three casesQ Mok, R Curley, J L Tolmie, et al.
Journal of Medical Genetics|April 16, 1998
Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestationA F Brady, P P Pandya, B Yuksel, et al.
British Heart Journal|December 1, 1992
Myocardial disarray in Noonan syndromeM Burch, J M Mann, M Sharland, et al.
Pageof 11

Showing results (71-80 of 110) with videos related to

Sort By:
Pageof 11
Clinical Dysmorphology|October 25, 2000
Further delineation of the DOOR syndromeA Rajab, A Riaz, G Paul, et al.
Journal of Medical Genetics|March 1, 1991
Floating-Harbor syndromeM A Patton, J Hurst, D Donnai, et al.
Clinical Genetics|March 3, 2009
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasiaM A Simpson, A Scheuerle, J Hurst, et al.
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.
Developmental Medicine and Child Neurology|February 1, 1997
Agenesis of the corpus callosum in Turner syndrome with ring XS E Abd, L Wilson, P Howlin, et al.
Genetic Testing|February 24, 2001
Novel mutations in the duplicated region of the polycystic kidney disease 1 (PKD1) gene provides supporting evidence for gene conversionA R Afzal, R N Florêncio, R Taylor, et al.
Journal of Medical Genetics|May 1, 1990
Restrictive dermopathy: a report of three casesQ Mok, R Curley, J L Tolmie, et al.
Journal of Medical Genetics|April 16, 1998
Outcome of chromosomally normal livebirths with increased fetal nuchal translucency at 10-14 weeks' gestationA F Brady, P P Pandya, B Yuksel, et al.
British Heart Journal|December 1, 1992
Myocardial disarray in Noonan syndromeM Burch, J M Mann, M Sharland, et al.
Pageof 11