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M A Patton

Showing results (41-50 of 110) with videos related to

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Journal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.
Lancet (London, England)|July 18, 1987
Use of DNA markers linked to cystic fibrosis gene to resolve equivocal sweat test resultsM A Patton, A Harris, C Quinlan, et al.
Journal of Medical Genetics|June 1, 1993
Congenital nystagmus cosegregating with a balanced 7;15 translocationM A Patton, S Jeffery, N Lee, et al.
Genetic Testing|April 19, 2002
Two families with blepharophimosis/ptosis/epicanthus inversus syndrome have mutations in the putative forkhead transcription factor FOXL2R Bell, V A Murday, M A Patton, et al.
Journal of Medical Genetics|January 14, 2000
A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)K Heathcote, P Syrris, N D Carter, et al.
Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.
Journal of Medical Genetics|May 1, 1992
Brachydactyly type C associated with shortening of the halluxJ M Rowe-Jones, A L Moss, M A Patton
Journal of Tropical Pediatrics|November 20, 1998
Neural tube defects and congenital hydrocephalus in the Sultanate of OmanA Rajab, A Vaishnav, N V Freeman, et al.
American Journal of Human Genetics|October 1, 1994
Non-Mendelian transmission in a human developmental disorder: split hand/split footG P Jarvik, M A Patton, T Homfray, et al.
American Journal of Medical Genetics|February 15, 1993
Genetic counselling in Noonan syndromeM Sharland, M Morgan, G Smith, et al.
Pageof 11

Showing results (41-50 of 110) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.
Lancet (London, England)|July 18, 1987
Use of DNA markers linked to cystic fibrosis gene to resolve equivocal sweat test resultsM A Patton, A Harris, C Quinlan, et al.
Journal of Medical Genetics|June 1, 1993
Congenital nystagmus cosegregating with a balanced 7;15 translocationM A Patton, S Jeffery, N Lee, et al.
Genetic Testing|April 19, 2002
Two families with blepharophimosis/ptosis/epicanthus inversus syndrome have mutations in the putative forkhead transcription factor FOXL2R Bell, V A Murday, M A Patton, et al.
Journal of Medical Genetics|January 14, 2000
A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)K Heathcote, P Syrris, N D Carter, et al.
Journal of Medical Genetics|April 1, 1985
The clinical features of the Cohen syndrome: further case reportsC North, M A Patton, M Baraitser, et al.
Journal of Medical Genetics|May 1, 1992
Brachydactyly type C associated with shortening of the halluxJ M Rowe-Jones, A L Moss, M A Patton
Journal of Tropical Pediatrics|November 20, 1998
Neural tube defects and congenital hydrocephalus in the Sultanate of OmanA Rajab, A Vaishnav, N V Freeman, et al.
American Journal of Human Genetics|October 1, 1994
Non-Mendelian transmission in a human developmental disorder: split hand/split footG P Jarvik, M A Patton, T Homfray, et al.
American Journal of Medical Genetics|February 15, 1993
Genetic counselling in Noonan syndromeM Sharland, M Morgan, G Smith, et al.
Pageof 11