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M A Patton

Showing results (31-40 of 110) with videos related to

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Clinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M Brett
American Journal of Medical Genetics|October 21, 1999
Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung diseaseP Syrris, N D Carter, M A Patton
Journal of Medical Genetics|October 1, 1995
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24H S Harrar, S Jeffery, M A Patton
Prenatal Diagnosis|August 1, 1997
Limb defects as a consequence of CVS or uterine lavage? A need for further documentation of the technique and complicationsY P Daryani, G Barker, M A Patton
Prenatal Diagnosis|March 1, 1997
Detection of cells of fetal origin from transcervical irrigationsY P Daryani, L K Penna, M A Patton
BMJ (Clinical Research Ed.)|May 7, 1994
Autosomal dominant polycystic kidney diseaseA K Saggar-Malik, S Jeffery, M A Patton
European Journal of Pediatrics|August 1, 1995
Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritanceD Lacombe, M A Patton, C Elleau, et al.
Clinical Genetics|March 1, 1991
Cutaneous lymphangioma and amegakaryocytic thrombocytopenia in Noonan syndromeD G Evans, R N Lonsdale, M A Patton
Lancet (London, England)|January 25, 1992
Long QT and Harvey-rasS Jeffery, R Jamieson, M A Patton, et al.
Journal of Medical Genetics|March 1, 1992
Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locusM Sharland, R Taylor, M A Patton, et al.
Pageof 11

Showing results (31-40 of 110) with videos related to

Sort By:
Pageof 11
Clinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M Brett
American Journal of Medical Genetics|October 21, 1999
Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung diseaseP Syrris, N D Carter, M A Patton
Journal of Medical Genetics|October 1, 1995
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24H S Harrar, S Jeffery, M A Patton
Prenatal Diagnosis|August 1, 1997
Limb defects as a consequence of CVS or uterine lavage? A need for further documentation of the technique and complicationsY P Daryani, G Barker, M A Patton
Prenatal Diagnosis|March 1, 1997
Detection of cells of fetal origin from transcervical irrigationsY P Daryani, L K Penna, M A Patton
BMJ (Clinical Research Ed.)|May 7, 1994
Autosomal dominant polycystic kidney diseaseA K Saggar-Malik, S Jeffery, M A Patton
European Journal of Pediatrics|August 1, 1995
Floating-Harbor syndrome: description of a further patient, review of the literature, and suggestion of autosomal dominant inheritanceD Lacombe, M A Patton, C Elleau, et al.
Clinical Genetics|March 1, 1991
Cutaneous lymphangioma and amegakaryocytic thrombocytopenia in Noonan syndromeD G Evans, R N Lonsdale, M A Patton
Lancet (London, England)|January 25, 1992
Long QT and Harvey-rasS Jeffery, R Jamieson, M A Patton, et al.
Journal of Medical Genetics|March 1, 1992
Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locusM Sharland, R Taylor, M A Patton, et al.
Pageof 11