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Human Genetics
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June 29, 1976
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain
G Ricco, U Mazza, R M Turi, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 17, 1989
[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]
M Losekoot, C Beijer, P C Giordano, et al.
The Journal of Biological Chemistry
|
March 17, 1995
cDNA sequence and expression of the ceratotoxin gene encoding an antibacterial sex-specific peptide from the medfly Ceratitis capitata (diptera)
D Marchini, A G Manetti, M Rosetto, et al.
American Journal of Obstetrics and Gynecology
|
January 1, 1987
Fetal blood group determination in first-trimester pregnancy for the management of severe immunization
H H Kanhai, J B Gravenhorst, R J Gemke, et al.
Human Genetics
|
September 1, 1997
alpha-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutations
K L Harteveld, M Losekoot, A J Heister, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
April 22, 1989
[Prenatal fetal blood group determination using chorionic villi biopsy]
H H Kanhai, R J Gemke, M A Overbeeke, et al.
Brain : a Journal of Neurology
|
September 1, 1980
Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study
C J Höweler, H F Busch, L F Bernini, et al.
Anticancer Research
|
September 1, 1992
Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer
N S Pellegata, M Losekoot, R Fodde, et al.
Journal of Medical Genetics
|
April 1, 1991
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene
M Losekoot, R Fodde, C L Harteveld, et al.
Hemoglobin
|
January 1, 1994
Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia
P C Giordano, C L Harteveld, H Streng, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 73) with videos related to
Sort By:
Page
of 8
Human Genetics
|
June 29, 1976
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain
G Ricco, U Mazza, R M Turi, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 17, 1989
[Combined alpha and beta thalassemia in a Chinese family in The Netherlands]
M Losekoot, C Beijer, P C Giordano, et al.
The Journal of Biological Chemistry
|
March 17, 1995
cDNA sequence and expression of the ceratotoxin gene encoding an antibacterial sex-specific peptide from the medfly Ceratitis capitata (diptera)
D Marchini, A G Manetti, M Rosetto, et al.
American Journal of Obstetrics and Gynecology
|
January 1, 1987
Fetal blood group determination in first-trimester pregnancy for the management of severe immunization
H H Kanhai, J B Gravenhorst, R J Gemke, et al.
Human Genetics
|
September 1, 1997
alpha-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutations
K L Harteveld, M Losekoot, A J Heister, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
April 22, 1989
[Prenatal fetal blood group determination using chorionic villi biopsy]
H H Kanhai, R J Gemke, M A Overbeeke, et al.
Brain : a Journal of Neurology
|
September 1, 1980
Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study
C J Höweler, H F Busch, L F Bernini, et al.
Anticancer Research
|
September 1, 1992
Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer
N S Pellegata, M Losekoot, R Fodde, et al.
Journal of Medical Genetics
|
April 1, 1991
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene
M Losekoot, R Fodde, C L Harteveld, et al.
Hemoglobin
|
January 1, 1994
Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia
P C Giordano, C L Harteveld, H Streng, et al.
Page
of 8