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Results of search for 'au:"Metzenberg, A B"'
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Authors
Chishti, A H
Das, S
Ettinger, T
Francisco, D L
Gitschier, J
Gregg, R G
Heiss, N
Hogan, K
Huisman, T H
Khaleghi, M
Kim, A C
Klauck, S M
Laxova, R
Marfatia, S M
McCutcheon, I E
Metcalfe, J
Metzenberg, A B
Pai, G S
Pan, Y
Poustka, A
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Topics
Amino Acid Sequence
Animals
Basal Ganglia Diseases
Base Sequence
Blood Proteins
Blotting, Southern
Body Weight
Bone and Bones
Chick Embryo
Chromosome Mapping
DNA
Factor VIII
Humans
Membrane Proteins
Molecular Sequence Data
Mutation
Oxygen
Syndrome
X Chromosome
genetics
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English
Your search returned 8 results.
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1.
The gene encoding the palmitoylated erythrocyte membrane protein, p55, originates at the CpG island 3' to the factor VIII gene.
[electronic resource]
by
Metzenberg, A B
Gitschier, J
Producer:
19930528
In:
Human molecular genetics
vol. 1
Online resources:
Available from publisher's website
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2.
Homology requirements for unequal crossing over in humans.
[electronic resource]
by
Metzenberg, A B
Wurzer, G
Huisman, T H
Smithies, O
Producer:
19910805
In:
Genetics
vol. 128
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3.
Organ growth in hyperoxic and hypoxic chick embryos.
[electronic resource]
by
McCutcheon, I E
Metcalfe, J
Metzenberg, A B
Ettinger, T
Producer:
19830311
In:
Respiration physiology
vol. 50
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4.
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter.
[electronic resource]
by
Gregg, R G
Metzenberg, A B
Hogan, K
Sekhon, G
Laxova, R
Producer:
19910702
In:
Genomics
vol. 9
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5.
Molecular evidence that the p55 gene is not responsible for either of two Xq28-linked disorders: Emery-Dreifuss muscular dystrophy and dyskeratosis congenita.
[electronic resource]
by
Metzenberg, A B
Pan, Y
Das, S
Pai, G S
Gitschier, J
Producer:
19940603
In:
American journal of human genetics
vol. 54
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6.
Oxygen availability and growth of the chick embryo.
[electronic resource]
by
Metcalfe, J
McCutcheon, I E
Francisco, D L
Metzenberg, A B
Welch, J E
Producer:
19820521
In:
Respiration physiology
vol. 46
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7.
Complete genomic organization of the human erythroid p55 gene (MPP1), a membrane-associated guanylate kinase homologue.
[electronic resource]
by
Kim, A C
Metzenberg, A B
Sahr, K E
Marfatia, S M
Chishti, A H
Producer:
19970304
In:
Genomics
vol. 31
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8.
Novel mutations of the DKC1 gene in individuals affected with dyskeratosis congenita.
[electronic resource]
by
Rostamiani, K
Klauck, S M
Heiss, N
Poustka, A
Khaleghi, M
Rosales, R
Metzenberg, A B
Producer:
20100413
In:
Blood cells, molecules & diseases
vol. 44
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