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Results of search for 'au:"NUSSBAUM, R"', page 6 of 9
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Authors
Airhart, S D
Bernard, D J
Caskey, C T
Chik, L
Dreyfuss, G
Dutra, A
Jänne, P A
Ledbetter, D H
Ledbetter, S A
Lesko, J G
Lewis, R A
Lin, T
NUSSBAUM, R
Nussbaum, R
Nussbaum, R H
Nussbaum, R L
Okabe, I
Polymeropoulos, M H
Puck, J M
Suchy, S F
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Adult
Animals
Base Sequence
Cell Line
Chromosome Mapping
Cloning, Molecular
DNA
Female
Genetic Linkage
Genetic Markers
Humans
Hybrid Cells
Male
Mice
Molecular Sequence Data
Nerve Tissue Proteins
Pedigree
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genetics
metabolism
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Your search returned 179 results.
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Results
101.
Cognitive deficits in a murine model of the eosinophilia-myalgia syndrome: a preliminary report.
[electronic resource]
by
Middaugh, L D
Nussbaum, R
Ludwicka, A
Bolster, M B
Silver, R M
Producer:
19970206
In:
Neurotoxicology and teratology
vol. 18
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102.
Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm.
[electronic resource]
by
Purrello, M
Nussbaum, R
Rinaldi, A
Filippi, G
Traccis, S
Latte, B
Siniscalco, M
Producer:
19840330
In:
Human genetics
vol. 65
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103.
Human hypoxanthine-guanine phosphoribosyltransferase. Detection of a mutant allele by restriction endonuclease analysis.
[electronic resource]
by
Wilson, J M
Frossard, P
Nussbaum, R L
Caskey, C T
Kelley, W N
Producer:
19831021
In:
The Journal of clinical investigation
vol. 72
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104.
Newborn screening for sickling hemoglobinopathies. Houston, 1976 to 1980.
[electronic resource]
by
Nussbaum, R L
Powell, C
Graham, H L
Caskey, C T
Fernbach, D J
Producer:
19840214
In:
American journal of diseases of children (1960)
vol. 138
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105.
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.
[electronic resource]
by
Nussbaum, R L
Orrison, B M
Jänne, P A
Charnas, L
Chinault, A C
Producer:
19970326
In:
Human genetics
vol. 99
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106.
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresis.
[electronic resource]
by
Schnur, R E
Knowlton, R G
Musarella, M A
Muenke, M
Nussbaum, R L
Producer:
19910116
In:
Genomics
vol. 8
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107.
Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: a systematic determination of cocloning rate and X-chromosome representation.
[electronic resource]
by
Lee, J T
Murgia, A
Sosnoski, D M
Olivos, I M
Nussbaum, R L
Producer:
19920514
In:
Genomics
vol. 12
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108.
Report of the third international workshop on human chromosome 22 mapping.
[electronic resource]
by
Emanuel, B S
Buetow, K
Nussbaum, R
Scambler, P
Lipinski, M
Overton, G C
Producer:
19930625
In:
Cytogenetics and cell genetics
vol. 63
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109.
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
[electronic resource]
by
Lin, T
Orrison, B M
Suchy, S F
Lewis, R A
Nussbaum, R L
Producer:
19981006
In:
Molecular genetics and metabolism
vol. 64
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110.
Disrupted sperm function and fertilin beta processing in mice deficient in the inositol polyphosphate 5-phosphatase Inpp5b.
[electronic resource]
by
Hellsten, E
Evans, J P
Bernard, D J
Jänne, P A
Nussbaum, R L
Producer:
20020214
In:
Developmental biology
vol. 240
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111.
ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation.
[electronic resource]
by
Schneider-Gädicke, A
Beer-Romero, P
Brown, L G
Nussbaum, R
Page, D C
Producer:
19890804
In:
Cell
vol. 57
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112.
Characterization and use of cloned sequences of the hypoxanthine-guanine phosphoribosyltransferase gene.
[electronic resource]
by
Chinault, A C
Brennand, J
Konecki, D S
Nussbaum, R L
Caskey, C T
Producer:
19840606
In:
Advances in experimental medicine and biology
vol. 165 Pt A
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113.
Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome.
[electronic resource]
by
Oakey, R J
Matteson, P G
Litwin, S
Tilghman, S M
Nussbaum, R L
Producer:
19960723
In:
Genetics
vol. 141
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114.
Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.
[electronic resource]
by
May, M
Colleaux, L
Murgia, A
Aylsworth, A
Nussbaum, R
Fontes, M
Schwartz, C
Producer:
19951215
In:
Human molecular genetics
vol. 4
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115.
First report of prenatal biochemical diagnosis of Lowe syndrome.
[electronic resource]
by
Suchy, S F
Lin, T
Horwitz, J A
O'Brien, W E
Nussbaum, R L
Producer:
19990305
In:
Prenatal diagnosis
vol. 18
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116.
Report of the committee on the genetic constitution of the X chromosome.
[electronic resource]
by
Mandel, J L
Willard, H F
Nussbaum, R L
Davies, K E
Romeo, G
Producer:
19890209
In:
Cytogenetics and cell genetics
vol. 49
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117.
Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 region.
[electronic resource]
by
Schnur, R E
Wick, P A
Sosnoski, D N
Bick, D
Nussbaum, R L
Producer:
19930511
In:
Genomics
vol. 15
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118.
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
[electronic resource]
by
Schnur, R E
Ledbetter, S A
Ledbetter, D H
Merry, D E
Nussbaum, R L
Producer:
19890216
In:
American journal of human genetics
vol. 44
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119.
The Gardner syndrome. Significance of ocular features.
[electronic resource]
by
Lewis, R A
Crowder, W E
Eierman, L A
Nussbaum, R L
Ferrell, R E
Producer:
19841128
In:
Ophthalmology
vol. 91
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120.
Report of the committee on the genetic constitution of the X chromosome.
[electronic resource]
by
Davies, K E
Mandel, J L
Monaco, A P
Nussbaum, R L
Willard, H F
Producer:
19910412
In:
Cytogenetics and cell genetics
vol. 55
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