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Results of search for 'au:"Saunières, A"'
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Authors
Bastiani, F
Butori, C
Canivet, B
Desnuelle, C
Hieronimus, S
Lambert, J C
Monfort, M F
Narbonne, H
Paquis, V
Paquis-Flucklinger, V
Paul, R
Pellissier, J F
Perucca-Lostanlen, D
Santucci-Darmanin, S
Saunieres, A
Saunieres, A M
Saunières, A
Saunières, A M
Vague, P
Vialettes, B
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Topics
Adolescent
Adult
Aged
Base Sequence
Cell Cycle Proteins
Child
DNA, Mitochondrial
Deafness
Diabetes Mellitus
Female
Humans
Infant
Male
Middle Aged
Mutation
Syndrome
analysis
complications
genetics
pathology
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English
French
Your search returned 14 results.
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1.
[45X/46XY formula and male sterility].
[electronic resource]
by
Lambert, J C
Donzeau, M
Saunieres, A M
Producer:
19890317
In:
Bulletin de l'Association des anatomistes
vol. 71
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2.
[Expressivity of familial forms of Fraser syndrome].
[electronic resource]
by
Lambert, J C
Touitou, I
Paquis, V
Saunières, A M
Producer:
19890818
In:
Journal de genetique humaine
vol. 37
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3.
Rapid mapping of mitochondrial dna deletions by large-fragment PCR.
[electronic resource]
by
Paul, R
Santucci, S
Saunières, A
Desnuelle, C
Paquis-Flucklinger, V
Producer:
19961223
In:
Trends in genetics : TIG
vol. 12
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4.
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene.
[electronic resource]
by
Paquis-Flucklinger, V
Santucci-Darmanin, S
Paul, R
Saunières, A
Turc-Carel, C
Desnuelle, C
Producer:
19971208
In:
Genomics
vol. 44
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5.
Branchial dysplasia, mental deficiency, club feet, and inguinal herniae: a report of two further cases associated with paucity of interlobular bile ducts.
[electronic resource]
by
Lambert, J C
Saint-Paul, M C
Bastiani, F
Paquis, V
Saunieres, A M
Producer:
19900717
In:
Journal of medical genetics
vol. 27
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6.
Searching for A3243G mitochondrial DNA mutation in buccal mucosa in order to improve the screening of patients with mitochondrial diabetes.
[electronic resource]
by
Narbonne, H
Perucca-Lostanlen, D
Desnuelle, C
Vialettes, B
Saunières, A
Paquis-Flucklinger, V
Producer:
20011204
In:
European journal of endocrinology
vol. 145
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7.
Alternative splicing of hMSH4: two isoforms in testis and abnormal transcripts in somatic tissues.
[electronic resource]
by
Santucci-Darmanin, S
Paul, R
Michiels, J F
Saunières, A
Desnuelle, C
Paquis-Flucklinger, V
Producer:
19990513
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 10
Online resources:
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8.
[Detection and prevalence of mitochondrial genome mutations in diabetes].
[electronic resource]
by
Paquis-Flucklinger, V
Vialettes, B
Canivet, B
Freychet, P
Hieronimus, S
Vague, P
Saunières, A
Desnuelle, C
Producer:
19970917
In:
Journees annuelles de diabetologie de l'Hotel-Dieu
p. 25-31
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9.
[Biochemical and ultrastructural study of two familial cases of Winchester syndrome].
[electronic resource]
by
Lambert, J C
Jaffray, J Y
Michalski, J C
Ortonne, J P
Paquis, V
Saunières, A M
Producer:
19900410
In:
Journal de genetique humaine
vol. 37
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10.
Early-onset fatal encephalomyopathy associated with severe mtDNA depletion.
[electronic resource]
by
Paquis-Flucklinger, V
Pellissier, J F
Camboulives, J
Chabrol, B
Saunières, A
Monfort, M F
Giudicelli, H
Desnuelle, C
Producer:
19951109
In:
European journal of pediatrics
vol. 154
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11.
Importance of searching for mtDNA defects in patients with diabetes and hearing deficit.
[electronic resource]
by
Paquis-Flucklinger, V
Vialettes, B
Vague, P
Canivet, B
Hieronimus, S
Oliver, C
Pellissier, J F
Saunières, A
Desnuelle, C
Producer:
19980911
In:
Diabetologia
vol. 41
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12.
Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
[electronic resource]
by
Perucca-Lostanlen, D
Narbonne, H
Hernandez, J B
Staccini, P
Saunieres, A
Paquis-Flucklinger, V
Vialettes, B
Desnuelle, C
Producer:
20001214
In:
Biochemical and biophysical research communications
vol. 277
Online resources:
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13.
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions.
[electronic resource]
by
Paul, R
Desnuelle, C
Pouget, J
Pellissier, J F
Richelme, C
Monfort, M F
Butori, C
Saunieres, A
Paquis-Flucklinger, V
Producer:
20000918
In:
European journal of human genetics : EJHG
vol. 8
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14.
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness.
[electronic resource]
by
Perucca-Lostanlen, D
Taylor, R W
Narbonne, H
Mousson de Camaret, B
Hayes, C M
Saunieres, A
Paquis-Flucklinger, V
Turnbull, D M
Vialettes, B
Desnuelle, C
Producer:
20021231
In:
Biochimica et biophysica acta
vol. 1588
Online resources:
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