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American Journal of Respiratory Cell and Molecular Biology
|
March 1, 2000
Pulmonary hypoplasia in the myogenin null mouse embryo
B S Tseng, S T Cavin, F W Booth, et al.
The Journal of Pediatrics
|
June 1, 1975
Combined immunodeficiency and vaccine-related poliomyelitis in a child with cartilage-hair hypoplasia
F T Saulsbury, J A Winkelstein, L E Davis, et al.
The Journal of Pediatrics
|
January 1, 1987
Folinic acid therapy in treatment of dihydropteridine reductase deficiency
M Irons, H L Levy, M E O'Flynn, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1980
CSF neurotransmitter studies. An infant with ascorbic acid-responsive tyrosinemia
J W Stoerner, I J Butler, F H Morriss, et al.
American Journal of Human Genetics
|
April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes
G A Greenhaw, A Hebert, M E Duke-Woodside, et al.
Journal of Child Neurology
|
May 1, 1996
Severity of medical and neurologic complications as a determinant of neurodevelopmental outcome at 6 and 12 months in very low birth weight infants
A E Anderson, S R Wildin, M Woodside, et al.
American Journal of Medical Genetics
|
February 1, 1985
Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards
J T Hecht, F W Nelson, I J Butler, et al.
Neurology
|
December 1, 1993
Rapid-onset dystonia-parkinsonism
W B Dobyns, L J Ozelius, P L Kramer, et al.
Brain : a Journal of Neurology
|
February 5, 2003
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease
A Jordanova, P De Jonghe, C F Boerkoel, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
American Journal of Respiratory Cell and Molecular Biology
|
March 1, 2000
Pulmonary hypoplasia in the myogenin null mouse embryo
B S Tseng, S T Cavin, F W Booth, et al.
The Journal of Pediatrics
|
June 1, 1975
Combined immunodeficiency and vaccine-related poliomyelitis in a child with cartilage-hair hypoplasia
F T Saulsbury, J A Winkelstein, L E Davis, et al.
The Journal of Pediatrics
|
January 1, 1987
Folinic acid therapy in treatment of dihydropteridine reductase deficiency
M Irons, H L Levy, M E O'Flynn, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1980
CSF neurotransmitter studies. An infant with ascorbic acid-responsive tyrosinemia
J W Stoerner, I J Butler, F H Morriss, et al.
American Journal of Human Genetics
|
April 1, 1992
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes
G A Greenhaw, A Hebert, M E Duke-Woodside, et al.
Journal of Child Neurology
|
May 1, 1996
Severity of medical and neurologic complications as a determinant of neurodevelopmental outcome at 6 and 12 months in very low birth weight infants
A E Anderson, S R Wildin, M Woodside, et al.
American Journal of Medical Genetics
|
February 1, 1985
Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards
J T Hecht, F W Nelson, I J Butler, et al.
Neurology
|
December 1, 1993
Rapid-onset dystonia-parkinsonism
W B Dobyns, L J Ozelius, P L Kramer, et al.
Brain : a Journal of Neurology
|
February 5, 2003
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease
A Jordanova, P De Jonghe, C F Boerkoel, et al.
Page
of 9