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Annales De Dermatologie Et De Venereologie
|
May 14, 2013
[Leg ulcer associated with type I cryoglobulinaemia due to incipient B-cell lymphoma]
C Lacoste, T A Duong, J Dupuis, et al.
Nucleic Acids Research
|
October 20, 2017
The yeast 2-μm plasmid Raf protein contributes to plasmid inheritance by stabilizing the Rep1 and Rep2 partitioning proteins
Mary E McQuaid, Jordan B Pinder, Niroshaathevi Arumuggam, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 2017
[Next-generation DNA sequencing in clinical diagnostics]
C Lacoste, A Fabre, C Pécheux, et al.
Journal of Intellectual Disability Research : JIDR
|
September 30, 2011
Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation
S Corbani, E Chouery, J Fayyad, et al.
Developmental Cell
|
November 13, 2001
A viral phospholipase A2 is required for parvovirus infectivity
Z Zádori, J Szelei, M C Lacoste, et al.
Clinical Genetics
|
November 21, 2008
The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA
E P Kirk, V Malaty-Brevaud, N Martini, et al.
Annales De Dermatologie Et De Venereologie
|
August 20, 2025
Muir-Torre syndrome revealed by sebaceous carcinoma of the scrotum
D-M Loga, R Salle, B Cavelier-Balloy, et al.
Cell Death & Disease
|
September 21, 2013
The sodium/iodide symporter NIS is a transcriptional target of the p53-family members in liver cancer cells
F Guerrieri, S Piconese, C Lacoste, et al.
Neuropathology and Applied Neurobiology
|
May 11, 2017
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation
F Sauvestre, S Moutton, C Badens, et al.
Clinical Genetics
|
July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome
C Badens, C Lacoste, N Philip, et al.
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of 3
Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Annales De Dermatologie Et De Venereologie
|
May 14, 2013
[Leg ulcer associated with type I cryoglobulinaemia due to incipient B-cell lymphoma]
C Lacoste, T A Duong, J Dupuis, et al.
Nucleic Acids Research
|
October 20, 2017
The yeast 2-μm plasmid Raf protein contributes to plasmid inheritance by stabilizing the Rep1 and Rep2 partitioning proteins
Mary E McQuaid, Jordan B Pinder, Niroshaathevi Arumuggam, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 2017
[Next-generation DNA sequencing in clinical diagnostics]
C Lacoste, A Fabre, C Pécheux, et al.
Journal of Intellectual Disability Research : JIDR
|
September 30, 2011
Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation
S Corbani, E Chouery, J Fayyad, et al.
Developmental Cell
|
November 13, 2001
A viral phospholipase A2 is required for parvovirus infectivity
Z Zádori, J Szelei, M C Lacoste, et al.
Clinical Genetics
|
November 21, 2008
The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA
E P Kirk, V Malaty-Brevaud, N Martini, et al.
Annales De Dermatologie Et De Venereologie
|
August 20, 2025
Muir-Torre syndrome revealed by sebaceous carcinoma of the scrotum
D-M Loga, R Salle, B Cavelier-Balloy, et al.
Cell Death & Disease
|
September 21, 2013
The sodium/iodide symporter NIS is a transcriptional target of the p53-family members in liver cancer cells
F Guerrieri, S Piconese, C Lacoste, et al.
Neuropathology and Applied Neurobiology
|
May 11, 2017
In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation
F Sauvestre, S Moutton, C Badens, et al.
Clinical Genetics
|
July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome
C Badens, C Lacoste, N Philip, et al.
Page
of 3