Search research articles
Contact Us
Filters
Showing results (61-70 of 110) with videos related to
Page
of 11
Sort By:
Lancet (London, England)
|
January 4, 1992
Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndrome
M 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 patients
M 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 development
M 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 cystinuria
M Sharland, M Jones, M Bain, et al.
Journal of Medical Genetics
|
June 1, 1994
Genital tract function in men with Noonan syndrome
M 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 needs
A 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 study
A C Shaw, K Kalidas, A H Crosby, et al.
Pediatric Radiology
|
January 1, 1993
Abdominal ultrasound in Noonan syndrome: a study of 44 patients
C 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 disorder
I Pollock, S J Holmes, M A Patton, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 110) with videos related to
Sort By:
Page
of 11
Lancet (London, England)
|
January 4, 1992
Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndrome
M 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 patients
M 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 development
M 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 cystinuria
M Sharland, M Jones, M Bain, et al.
Journal of Medical Genetics
|
June 1, 1994
Genital tract function in men with Noonan syndrome
M 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 needs
A 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 study
A C Shaw, K Kalidas, A H Crosby, et al.
Pediatric Radiology
|
January 1, 1993
Abdominal ultrasound in Noonan syndrome: a study of 44 patients
C 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 disorder
I Pollock, S J Holmes, M A Patton, et al.
Page
of 11