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Results of search for 'au:"Bittel, D C"'
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Authors
Abdelmoity, A T
Andrews, G K
Bittel, D C
Brooks, W M
Butler, M G
Chambers, R
Cooley, L D
Fischer, W
Frisch, D A
Gengenbach, B G
Graf, W D
Gustafson, J P
Holsen, L M
Kibiryeva, N
Shaver, J M
Smirnova, I V
Somers, D A
Talebizadeh, Z
Theodoro, M F
Yu, S
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Adolescent
Adult
Alleles
Amino Acid Sequence
Animals
Autistic Disorder
Cell Line
Cells, Cultured
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 15
DNA Mutational Analysis
Female
Humans
Male
Prader-Willi Syndrome
Transcription Factors
genetics
metabolism
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English
Your search returned 15 results.
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1.
Dosage response of rye genes in a wheat background : 2. Secalin genes on 1RS.
[electronic resource]
by
Bittel, D C
Gustafson, J P
Producer:
20131111
In:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
vol. 84
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2.
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array.
[electronic resource]
by
Newkirk, H L
Bittel, D C
Butler, M G
Producer:
20080911
In:
American journal of medical genetics. Part A
vol. 146A
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3.
Functional heterogeneity in the zinc fingers of metalloregulatory protein metal response element-binding transcription factor-1.
[electronic resource]
by
Bittel, D C
Smirnova, I V
Andrews, G K
Producer:
20010108
In:
The Journal of biological chemistry
vol. 275
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4.
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.
[electronic resource]
by
Bittel, D C
Kibiryeva, N
Talebizadeh, Z
Butler, M G
Producer:
20031103
In:
Journal of medical genetics
vol. 40
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5.
Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase.
[electronic resource]
by
Bittel, D C
Shaver, J M
Somers, D A
Gengenbach, B G
Producer:
20131030
In:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik
vol. 92
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6.
Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1.
[electronic resource]
by
Smirnova, I V
Bittel, D C
Ravindra, R
Jiang, H
Andrews, G K
Producer:
20000504
In:
The Journal of biological chemistry
vol. 275
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7.
Brief report: non-random X chromosome inactivation in females with autism.
[electronic resource]
by
Talebizadeh, Z
Bittel, D C
Veatch, O J
Kibiryeva, N
Butler, M G
Producer:
20060321
In:
Journal of autism and developmental disorders
vol. 35
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8.
Comparison of X-chromosome inactivation patterns in multiple tissues from human females.
[electronic resource]
by
Bittel, D C
Theodoro, M F
Kibiryeva, N
Fischer, W
Talebizadeh, Z
Butler, M G
Producer:
20080716
In:
Journal of medical genetics
vol. 45
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9.
Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjects.
[electronic resource]
by
Kennedy, L
Bittel, D C
Kibiryeva, N
Kalra, S P
Torto, R
Butler, M G
Producer:
20061030
In:
International journal of obesity (2005)
vol. 30
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10.
Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
[electronic resource]
by
Graf, W D
Le Pichon, J-B
Bittel, D C
Abdelmoity, A T
Yu, S
Producer:
20100421
In:
Neurology
vol. 74
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11.
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
[electronic resource]
by
Talebizadeh, Z
Lam, D Y
Theodoro, M F
Bittel, D C
Lushington, G H
Butler, M G
Producer:
20060717
In:
Journal of medical genetics
vol. 43
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12.
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.
[electronic resource]
by
Bittel, D C
Yu, S
Newkirk, H
Kibiryeva, N
Holt, A
Butler, M G
Cooley, L D
Producer:
20090519
In:
Cytogenetic and genome research
vol. 124
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13.
No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD).
[electronic resource]
by
Talebizadeh, Z
Bittel, D C
Miles, J H
Takahashi, N
Wang, C H
Kibiryeva, N
Butler, M G
Producer:
20021119
In:
Journal of medical genetics
vol. 39
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14.
Single-amino acid substitutions eliminate lysine inhibition of maize dihydrodipicolinate synthase.
[electronic resource]
by
Shaver, J M
Bittel, D C
Sellner, J M
Frisch, D A
Somers, D A
Gengenbach, B G
Producer:
19960905
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 93
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15.
Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.
[electronic resource]
by
Holsen, L M
Zarcone, J R
Chambers, R
Butler, M G
Bittel, D C
Brooks, W M
Thompson, T I
Savage, C R
Producer:
20091014
In:
International journal of obesity (2005)
vol. 33
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