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M A Patton

Showing results (61-70 of 110) with videos related to

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Lancet (London, England)|January 4, 1992
Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndromeM Sharland, M A Patton, S Talbot, et al.
American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.
Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.
Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
Journal of Medical Genetics|July 1, 1992
Balanced translocation (14;20) in a mentally handicapped child with cystinuriaM Sharland, M Jones, M Bain, et al.
Journal of Medical Genetics|June 1, 1994
Genital tract function in men with Noonan syndromeM M Elsawi, J P Pryor, G Klufio, et al.
Journal of Community Genetics|March 4, 2014
Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needsA Rajab, Q Al Salmi, J Jaffer, et al.
Archives of Disease in Childhood|September 23, 2006
The natural history of Noonan syndrome: a long-term follow-up studyA C Shaw, K Kalidas, A H Crosby, et al.
Pediatric Radiology|January 1, 1993
Abdominal ultrasound in Noonan syndrome: a study of 44 patientsC D George, M A Patton, M el Sawi, et al.
Journal of Medical Genetics|July 1, 1991
Congenital intestinal pseudo-obstruction associated with a giant platelet disorderI Pollock, S J Holmes, M A Patton, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Lancet (London, England)|January 4, 1992
Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndromeM Sharland, M A Patton, S Talbot, et al.
American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.
Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.
Journal of Medical Genetics|September 1, 1987
Congenital cutis laxa with retardation of growth and developmentM A Patton, J Tolmie, P Ruthnum, et al.
Journal of Medical Genetics|July 1, 1992
Balanced translocation (14;20) in a mentally handicapped child with cystinuriaM Sharland, M Jones, M Bain, et al.
Journal of Medical Genetics|June 1, 1994
Genital tract function in men with Noonan syndromeM M Elsawi, J P Pryor, G Klufio, et al.
Journal of Community Genetics|March 4, 2014
Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needsA Rajab, Q Al Salmi, J Jaffer, et al.
Archives of Disease in Childhood|September 23, 2006
The natural history of Noonan syndrome: a long-term follow-up studyA C Shaw, K Kalidas, A H Crosby, et al.
Pediatric Radiology|January 1, 1993
Abdominal ultrasound in Noonan syndrome: a study of 44 patientsC D George, M A Patton, M el Sawi, et al.
Journal of Medical Genetics|July 1, 1991
Congenital intestinal pseudo-obstruction associated with a giant platelet disorderI Pollock, S J Holmes, M A Patton, et al.
Pageof 11