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Results of search for 'au:"LALANDE, M"', page 6 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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Undetermined
Your search returned 141 results.
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101.
Complications of abortion performed under local anesthesia.
[electronic resource]
by
Thonneau, P
Fougeyrollas, B
Ducot, B
Boubilley, D
Dif, J
Lalande, M
Soulat, C
Producer:
19990209
In:
European journal of obstetrics, gynecology, and reproductive biology
vol. 81
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102.
[Pseudotumoral-like recurrence of visceral leishmaniasis in a seven-year-old girl].
[electronic resource]
by
Jeziorski, E
Blanchet, C
Ludwig, C
Lalande, M
Coste, V
Dereure, J
Rodière, M
Producer:
20100108
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 16 Suppl 2
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103.
Washin and washout of isoflurane during cardiopulmonary bypass.
[electronic resource]
by
Henderson, J M
Nathan, H J
Lalande, M
Winkler, M H
Dubé, L M
Producer:
19890202
In:
Canadian journal of anaesthesia = Journal canadien d'anesthesie
vol. 35
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104.
[Intravenous immunoglobulin-resistant Kawasaki disease with hemophagocytosis].
[electronic resource]
by
Servel, A-C
Vincenti, M
Darras, J-P
Lalande, M
Rodière, M
Filleron, A
Producer:
20121113
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 19
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105.
Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.
[electronic resource]
by
Lalande, M
Donlon, T
Petersen, R A
Liberfarb, R
Manter, S
Latt, S A
Producer:
19861118
In:
Cancer genetics and cytogenetics
vol. 23
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106.
Usage of the flow cytometer-cell sorter.
[electronic resource]
by
Miller, R G
Lalande, M E
McCutcheon, M J
Stewart, S S
Price, G B
Producer:
19820222
In:
Journal of immunological methods
vol. 47
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107.
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.
[electronic resource]
by
Wagstaff, J
Knoll, J H
Glatt, K A
Shugart, Y Y
Sommer, A
Lalande, M
Producer:
19930609
In:
Nature genetics
vol. 1
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108.
Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci.
[electronic resource]
by
Kunkel, L M
Lalande, M
Monaco, A P
Flint, A
Middlesworth, W
Latt, S A
Producer:
19850809
In:
Gene
vol. 33
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109.
Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locus.
[electronic resource]
by
Lalande, M
Dryja, T P
Schreck, R R
Shipley, J
Flint, A
Latt, S A
Producer:
19850131
In:
Cancer genetics and cytogenetics
vol. 13
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110.
Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene.
[electronic resource]
by
Saitoh, S
Kubota, T
Ohta, T
Jinno, Y
Niikawa, N
Sugimoto, T
Wagstaff, J
Lalande, M
Producer:
19920303
In:
Lancet (London, England)
vol. 339
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111.
Deletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) females.
[electronic resource]
by
Müller, U
Donlon, T
Schmid, M
Fitch, N
Richer, C L
Lalande, M
Latt, S A
Producer:
19861015
In:
Nucleic acids research
vol. 14
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112.
[CLINICAL AND BIOLOGICAL STUDY OF A CASE OF PHEOCHROMOCYTOMA].
[electronic resource]
by
LAMY, M
FREZAL, J
REY, J
FAURE, C
PELLERIN, D
PHILIPPART, M
NEZELOF, C
LALANDE, M
Producer:
19961201
In:
Archives francaises de pediatrie
vol. 21
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113.
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
[electronic resource]
by
Ozçelik, T
Leff, S
Robinson, W
Donlon, T
Lalande, M
Sanjines, E
Schinzel, A
Francke, U
Producer:
19930623
In:
Nature genetics
vol. 2
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114.
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
[electronic resource]
by
Reis, A
Dittrich, B
Greger, V
Buiting, K
Lalande, M
Gillessen-Kaesbach, G
Anvret, M
Horsthemke, B
Producer:
19940603
In:
American journal of human genetics
vol. 54
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115.
The human T cell receptor alpha-delta locus: a physical map of the variable, joining and constant region genes.
[electronic resource]
by
Griesser, H
Champagne, E
Tkachuk, D
Takihara, Y
Lalande, M
Baillie, E
Minden, M
Mak, T W
Producer:
19880623
In:
European journal of immunology
vol. 18
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116.
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
[electronic resource]
by
Knoll, J H
Nicholls, R D
Magenis, R E
Graham, J M
Lalande, M
Latt, S A
Producer:
19890427
In:
American journal of medical genetics
vol. 32
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117.
[Quality of life in HIV-infected children and adolescents under highly active antiretroviral therapy: change over time, effects of age and familial context].
[electronic resource]
by
Thöni, G J
Lalande, M
Bachelard, G
Vidal, P
Manificat, S
Fédou, C
Rodière, M
Nicolas, J
Producer:
20060323
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 13
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118.
Inhibition of the G1-S transition of the cell cycle by inhibitors of deoxyhypusine hydroxylation.
[electronic resource]
by
Hanauske-Abel, H M
Park, M H
Hanauske, A R
Popowicz, A M
Lalande, M
Folk, J E
Producer:
19940506
In:
Biochimica et biophysica acta
vol. 1221
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119.
Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13.
[electronic resource]
by
Webb, T
Clayton-Smith, J
Cheng, X J
Knoll, J H
Lalande, M
Pembrey, M E
Malcolm, S
Producer:
19930209
In:
Journal of medical genetics
vol. 29
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120.
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene.
[electronic resource]
by
Buiting, K
Dittrich, B
Gross, S
Greger, V
Lalande, M
Robinson, W
Mutirangura, A
Ledbetter, D
Horsthemke, B
Producer:
19940331
In:
Human molecular genetics
vol. 2
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