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Neuropediatrics
|
November 1, 1988
Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system
N Illum, E Reske-Nielsen, F Skovby, et al.
The British Journal of Ophthalmology
|
September 1, 1992
Concurrent uveoretinitis and pineocytoma in a child suggests a causal relationship
N Illum, H W Korf, K Julian, et al.
Neuropediatrics
|
May 1, 1990
Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndrome
N Illum, K Taudorf, C Heilmann, et al.
Child Nephrology and Urology
|
January 1, 1992
Primary hyperoxaluria type 1: clinical manifestations in infancy and prenatal diagnosis
N Illum, L Lavard, C J Danpure, et al.
Blood
|
March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia
W Tang, S P Cai, B Eng, et al.
Blood
|
February 1, 1994
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]
S F Parsons, J Jones, D J Anstee, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome
Z Tümer, A M Henriksen, I Bache, et al.
Scandinavian Journal of Infectious Diseases
|
January 1, 1994
The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis
K Hjelt, N Højlyng, P Howitz, et al.
The Journal of Clinical Investigation
|
September 1, 1994
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia
P Agre, B L Smith, R Baumgarten, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Neuropediatrics
|
November 1, 1988
Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system
N Illum, E Reske-Nielsen, F Skovby, et al.
The British Journal of Ophthalmology
|
September 1, 1992
Concurrent uveoretinitis and pineocytoma in a child suggests a causal relationship
N Illum, H W Korf, K Julian, et al.
Neuropediatrics
|
May 1, 1990
Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndrome
N Illum, K Taudorf, C Heilmann, et al.
Child Nephrology and Urology
|
January 1, 1992
Primary hyperoxaluria type 1: clinical manifestations in infancy and prenatal diagnosis
N Illum, L Lavard, C J Danpure, et al.
Blood
|
March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia
W Tang, S P Cai, B Eng, et al.
Blood
|
February 1, 1994
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]
S F Parsons, J Jones, D J Anstee, et al.
American Journal of Medical Genetics. Part A
|
May 12, 2005
Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome
Z Tümer, A M Henriksen, I Bache, et al.
Scandinavian Journal of Infectious Diseases
|
January 1, 1994
The role of Mycobacteria Other Than Tuberculosis (MOTT) in patients with cystic fibrosis
K Hjelt, N Højlyng, P Howitz, et al.
The Journal of Clinical Investigation
|
September 1, 1994
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia
P Agre, B L Smith, R Baumgarten, et al.
Page
of 2