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Acta Paediatrica Scandinavica
|
January 1, 1991
The relation between perinatal conditions and developmental outcome in low birthweight infants. Comparison of two cohorts
P H Ellison, G Greisen, M Foster, et al.
Veterinary Journal (London, England : 1997)
|
June 28, 2024
Serum Amyloid A and Haptoglobin concentrations in calves at first event of respiratory disease were not associated with subsequent risk of respiratory disease during the preweaning period
H H Møller, M B Petersen, M A Krogh, et al.
Annales De Genetique
|
January 1, 1989
A case of the ring 20 syndrome
S G Thomsen, M B Petersen, E A Andersen, et al.
Clinical Genetics
|
January 1, 1994
Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regions
A M Gerdes, M B Petersen, H D Schrøder, et al.
Genomics
|
May 1, 1990
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker
M B Petersen, E P Economou, S A Slaugenhaupt, et al.
American Journal of Human Genetics
|
December 1, 1990
Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations
S E Antonarakis, P A Adelsberger, M B Petersen, et al.
British Medical Journal (Clinical Research Ed.)
|
February 27, 1988
Early growth delay in diabetic pregnancy: relation to psychomotor development at age 4
M B Petersen, S A Pedersen, G Greisen, et al.
Human Mutation
|
June 30, 2000
Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness
T Antoniadi, K Grønskov, A Sand, et al.
Journal of Medical Genetics
|
October 1, 1992
Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q
C A Brandt, J M Hertz, M B Petersen, et al.
Genomics
|
June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21
M B Petersen, O Bartsch, P A Adelsberger, et al.
Page
of 17
Search research articles
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Showing results (71-80 of 161) with videos related to
Sort By:
Page
of 17
Acta Paediatrica Scandinavica
|
January 1, 1991
The relation between perinatal conditions and developmental outcome in low birthweight infants. Comparison of two cohorts
P H Ellison, G Greisen, M Foster, et al.
Veterinary Journal (London, England : 1997)
|
June 28, 2024
Serum Amyloid A and Haptoglobin concentrations in calves at first event of respiratory disease were not associated with subsequent risk of respiratory disease during the preweaning period
H H Møller, M B Petersen, M A Krogh, et al.
Annales De Genetique
|
January 1, 1989
A case of the ring 20 syndrome
S G Thomsen, M B Petersen, E A Andersen, et al.
Clinical Genetics
|
January 1, 1994
Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regions
A M Gerdes, M B Petersen, H D Schrøder, et al.
Genomics
|
May 1, 1990
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker
M B Petersen, E P Economou, S A Slaugenhaupt, et al.
American Journal of Human Genetics
|
December 1, 1990
Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations
S E Antonarakis, P A Adelsberger, M B Petersen, et al.
British Medical Journal (Clinical Research Ed.)
|
February 27, 1988
Early growth delay in diabetic pregnancy: relation to psychomotor development at age 4
M B Petersen, S A Pedersen, G Greisen, et al.
Human Mutation
|
June 30, 2000
Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness
T Antoniadi, K Grønskov, A Sand, et al.
Journal of Medical Genetics
|
October 1, 1992
Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q
C A Brandt, J M Hertz, M B Petersen, et al.
Genomics
|
June 1, 1992
Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21
M B Petersen, O Bartsch, P A Adelsberger, et al.
Page
of 17