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M A Patton

Showing results (11-20 of 110) with videos related to

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Journal of Medical Genetics|July 1, 1993
Cutis laxa and the Costello syndromeM A Patton, M Baraitser
American Journal of Medical Genetics|November 6, 1995
Familial microtia with meatal atresia and conductive deafness in five generationsA Gupta, M A Patton
Community Genetics|June 5, 2004
Development and use of a national haemoglobinopathy register in OmanA Rajab, M A Patton
Journal of Medical Genetics|April 1, 1986
A Noonan-like short stature syndrome with sparse hairM Baraitser, M A Patton
Journal of Medical Genetics|May 16, 2002
Robinow syndromeM A Patton, A R Afzal
American Journal of Medical Genetics|September 6, 1996
Web-neck anomaly and its association with congenital heart diseaseA F Brady, M A Patton
Clinical Dysmorphology|November 14, 1997
Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome)--evidence for possible autosomal recessive inheritanceA F Brady, M A Patton
Journal of Medical Genetics|October 1, 1985
Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotypeM A Patton, K M Laurence
Journal of Medical Genetics|September 1, 1991
The frequency of mental retardation in hypochondroplasiaR Wynne-Davies, M A Patton
American Journal of Medical Genetics|June 15, 1991
Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2M Sharland, M A Patton, L Hill
Pageof 11

Showing results (11-20 of 110) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|July 1, 1993
Cutis laxa and the Costello syndromeM A Patton, M Baraitser
American Journal of Medical Genetics|November 6, 1995
Familial microtia with meatal atresia and conductive deafness in five generationsA Gupta, M A Patton
Community Genetics|June 5, 2004
Development and use of a national haemoglobinopathy register in OmanA Rajab, M A Patton
Journal of Medical Genetics|April 1, 1986
A Noonan-like short stature syndrome with sparse hairM Baraitser, M A Patton
Journal of Medical Genetics|May 16, 2002
Robinow syndromeM A Patton, A R Afzal
American Journal of Medical Genetics|September 6, 1996
Web-neck anomaly and its association with congenital heart diseaseA F Brady, M A Patton
Clinical Dysmorphology|November 14, 1997
Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome)--evidence for possible autosomal recessive inheritanceA F Brady, M A Patton
Journal of Medical Genetics|October 1, 1985
Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotypeM A Patton, K M Laurence
Journal of Medical Genetics|September 1, 1991
The frequency of mental retardation in hypochondroplasiaR Wynne-Davies, M A Patton
American Journal of Medical Genetics|June 15, 1991
Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2M Sharland, M A Patton, L Hill
Pageof 11