Search research articles
Contact Us
Filters
Showing results (1-10 of 45) with videos related to
Page
of 5
Sort By:
American Journal of Medical Genetics
|
July 31, 2001
Nablus mask-like facial syndrome
J Allanson
Journal of Medical Genetics
|
February 1, 1991
Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2
J Allanson, S Richter
American Journal of Medical Genetics
|
February 5, 1998
Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases"
T Cole, J Allanson
Clinical Genetics
|
February 1, 1986
Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethality
J Allanson, W Austin, F Hecht
American Journal of Medical Genetics
|
August 1, 1989
Child with deletion of 4q and duplication of 1q
J Wade, T Morgan, J Allanson
Journal of Medical Genetics
|
August 1, 1989
Familial translocation t(9;16)
C Dowman, D Lockwood, J Allanson
Journal of Medical Genetics
|
December 3, 2008
No reason yet to change diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes
G Neri, J Allanson, M I Kavamura
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 20, 2002
Characteristics of patients with persistent severe disability and medically unexplained neurological symptoms: a pilot study
J Allanson, C Bass, D T Wade
The New England Journal of Medicine
|
December 24, 1987
Aortic-root dilatation in Noonan's syndrome
A E Lin, K L Garver, J Allanson
Genetic Testing
|
January 1, 1997
Prenatal diagnosis in congenital contractural arachnodactyly
S Belleh, L Spooner, J Allanson, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
July 31, 2001
Nablus mask-like facial syndrome
J Allanson
Journal of Medical Genetics
|
February 1, 1991
Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2
J Allanson, S Richter
American Journal of Medical Genetics
|
February 5, 1998
Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases"
T Cole, J Allanson
Clinical Genetics
|
February 1, 1986
Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethality
J Allanson, W Austin, F Hecht
American Journal of Medical Genetics
|
August 1, 1989
Child with deletion of 4q and duplication of 1q
J Wade, T Morgan, J Allanson
Journal of Medical Genetics
|
August 1, 1989
Familial translocation t(9;16)
C Dowman, D Lockwood, J Allanson
Journal of Medical Genetics
|
December 3, 2008
No reason yet to change diagnostic criteria for Noonan, Costello and cardio-facio-cutaneous syndromes
G Neri, J Allanson, M I Kavamura
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 20, 2002
Characteristics of patients with persistent severe disability and medically unexplained neurological symptoms: a pilot study
J Allanson, C Bass, D T Wade
The New England Journal of Medicine
|
December 24, 1987
Aortic-root dilatation in Noonan's syndrome
A E Lin, K L Garver, J Allanson
Genetic Testing
|
January 1, 1997
Prenatal diagnosis in congenital contractural arachnodactyly
S Belleh, L Spooner, J Allanson, et al.
Page
of 5