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Results of search for 'au:"LALANDE, M"', page 5 of 8
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Authors
Buiting, K
Bélanger, P M
Donlon, T
Flint, A
Glatt, H
Glatt, K
Greger, V
Horsthemke, B
Knoll, J H
LaSalle, J M
Lalande, M
Lalande, M E
Latt, S A
Miller, R G
Müller, U
Nicholls, R D
Rodière, M
Sinnett, D
Turmel, C
Wagstaff, J
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Topics
Angelman Syndrome
Animals
Base Sequence
Cell Line
Chromosome Deletion
Chromosome Mapping
Chromosomes, Human, Pair 15
DNA
Female
Flow Cytometry
Genetic Markers
Genomic Imprinting
Humans
Male
Molecular Sequence Data
Prader-Willi Syndrome
analysis
genetics
metabolism
methods
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Your search returned 141 results.
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81.
Effects of X-irradiation on cell-cycle progression, induction of chromosomal aberrations and cell killing in ataxia telangiectasia (AT) fibroblasts.
[electronic resource]
by
Nagasawa, H
Latt, S A
Lalande, M E
Little, J B
Producer:
19850308
In:
Mutation research
vol. 148
Online resources:
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82.
Parental imprinting and Angelman syndrome.
[electronic resource]
by
Lalande, M
Minassian, B A
DeLorey, T M
Olsen, R W
Producer:
19991103
In:
Advances in neurology
vol. 79
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83.
Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14.
[electronic resource]
by
Strehl, S
Glatt, K
Liu, Q M
Glatt, H
Lalande, M
Producer:
19981211
In:
Genomics
vol. 53
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84.
Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.
[electronic resource]
by
Higgins, M J
Turmel, C
Noolandi, J
Neumann, P E
Lalande, M
Producer:
19900606
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 87
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85.
[Hypertension in the absence of renal involvement during childhood Henoch-Schönlein purpura].
[electronic resource]
by
Darteyre, S
Ludwig, C
Lalande, M
Rodière, M
Guillaumont, S
Morin, D
Producer:
20081002
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 15
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86.
[Consequences of exclusive breast-feeding in vegan mother newborn--case report].
[electronic resource]
by
Mariani, A
Chalies, S
Jeziorski, E
Ludwig, C
Lalande, M
Rodière, M
Producer:
20100119
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 16
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87.
Cell cycle distribution of chronically hypoxic cells and determination of the clonogenic potential of cells accumulated in G2 + M phases after irradiation of a solid tumor in vivo.
[electronic resource]
by
Pallavicini, M G
Lalande, M E
Miller, R G
Hill, R P
Producer:
19790829
In:
Cancer research
vol. 39
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88.
Applications of fluorescence spectroscopy to molecular cytogenetics.
[electronic resource]
by
Latt, S A
Lalande, M
Kunkel, L M
Schreck, R
Tantravahi, U
Producer:
19850620
In:
Biopolymers
vol. 24
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89.
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.
[electronic resource]
by
Donlon, T A
Lalande, M
Wyman, A
Bruns, G
Latt, S A
Producer:
19860718
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 83
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90.
[Group B streptococcal infection with 2 recurrences in a newborn].
[electronic resource]
by
Lalande, M
Marchandin, H
Enaud, L
Carrière, C
Rodière, M
Astruc, J
Producer:
20020318
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 9
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91.
[Eruptive pseudoangiomatosis in infant and newborns].
[electronic resource]
by
Guillot, B
Chraibi, H
Girard, C
Dereure, O
Lalande, M
Bessis, D
Producer:
20060224
In:
Annales de dermatologie et de venereologie
vol. 132
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92.
Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.
[electronic resource]
by
Harris, P
Lalande, M
Stroh, H
Bruns, G
Flint, A
Latt, S A
Producer:
19871117
In:
Human genetics
vol. 77
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93.
The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.
[electronic resource]
by
Boccaccio, I
Glatt-Deeley, H
Watrin, F
Roëckel, N
Lalande, M
Muscatelli, F
Producer:
20000124
In:
Human molecular genetics
vol. 8
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94.
Isolation and structural characterization by spectroscopic methods of two glucuronide metabolites of mexiletine after N-oxidation and deamination.
[electronic resource]
by
Turgeon, J
Paré, J R
Lalande, M
Grech-Bélanger, O
Bélanger, P M
Producer:
19921223
In:
Drug metabolism and disposition: the biological fate of chemicals
vol. 20
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95.
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
[electronic resource]
by
Nicholls, R D
Knoll, J H
Butler, M G
Karam, S
Lalande, M
Producer:
19891221
In:
Nature
vol. 342
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96.
Scrambling of bands in gel electrophoresis of DNA.
[electronic resource]
by
Lalande, M
Noolandi, J
Turmel, C
Brousseau, R
Rousseau, J
Slater, G W
Producer:
19880811
In:
Nucleic acids research
vol. 16
Online resources:
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97.
Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.
[electronic resource]
by
Knoll, J H
Glatt, K A
Nicholls, R D
Malcolm, S
Lalande, M
Producer:
19910205
In:
American journal of human genetics
vol. 48
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98.
Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism.
[electronic resource]
by
Müller, U
Donlon, T A
Kunkel, S M
Lalande, M
Latt, S A
Producer:
19870414
In:
Human genetics
vol. 75
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99.
High resolution analysis of the timing of replication of specific DNA sequences during S phase of mammalian cells.
[electronic resource]
by
D'Andrea, A D
Tantravahi, U
Lalande, M
Perle, M A
Latt, S A
Producer:
19830920
In:
Nucleic acids research
vol. 11
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100.
High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients.
[electronic resource]
by
Sinnett, D
Wagstaff, J
Glatt, K
Woolf, E
Kirkness, E J
Lalande, M
Producer:
19930701
In:
American journal of human genetics
vol. 52
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