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Bulletin of Environmental Contamination and Toxicology
|
April 1, 1984
Organochlorine residue levels in Mississippi River water snakes in southern Louisiana
T D Sabourin, W B Stickle, T C Michot, et al.
The European Journal of Medicine
|
October 1, 1993
Treatment of multiple myeloma with etidronate: results of a multicentre double-blind study. Groupe d'Etudes et de Recherches sur le Myélome (GERM)
A Daragon, C Humez, C Michot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 25, 2017
[About twins: Epidemiological, genetic, and obstetrical aspects, specific risks, and outcome]
M Tauzin, A Felix, C Michot, et al.
Journal of Stomatology, Oral and Maxillofacial Surgery
|
January 15, 2019
Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategies
G Marechal, T Schouman, C Mauprivez, et al.
Ecology and Evolution
|
May 22, 2023
Multiple lines of evidence suggest the persistence of the Ivory-billed Woodpecker (<i>Campephilus principalis</i>) in Louisiana
Steven C Latta, Mark A Michaels, Thomas C Michot, et al.
Arthritis and Rheumatism
|
January 22, 2000
Evolution of chronic recurrent multifocal osteitis toward spondylarthropathy over the long term
O Vittecoq, L A Said, C Michot, et al.
European Journal of Medical Genetics
|
July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid
M Essaoui, M Nizon, M P Beaujard, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2022
SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients
M Mouillé, M Rio, S Breton, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
May 18, 2026
Characteristics and outcomes of patients with pediatric-onset non-mastocytosis mast cell activation disorders: A CEREMAST study
M Weiss, J Rossignol, F Campeotto, et al.
Clinical Genetics
|
December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome
M Nizon, M Henry, C Michot, et al.
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of 5
Search research articles
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Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Bulletin of Environmental Contamination and Toxicology
|
April 1, 1984
Organochlorine residue levels in Mississippi River water snakes in southern Louisiana
T D Sabourin, W B Stickle, T C Michot, et al.
The European Journal of Medicine
|
October 1, 1993
Treatment of multiple myeloma with etidronate: results of a multicentre double-blind study. Groupe d'Etudes et de Recherches sur le Myélome (GERM)
A Daragon, C Humez, C Michot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 25, 2017
[About twins: Epidemiological, genetic, and obstetrical aspects, specific risks, and outcome]
M Tauzin, A Felix, C Michot, et al.
Journal of Stomatology, Oral and Maxillofacial Surgery
|
January 15, 2019
Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategies
G Marechal, T Schouman, C Mauprivez, et al.
Ecology and Evolution
|
May 22, 2023
Multiple lines of evidence suggest the persistence of the Ivory-billed Woodpecker (<i>Campephilus principalis</i>) in Louisiana
Steven C Latta, Mark A Michaels, Thomas C Michot, et al.
Arthritis and Rheumatism
|
January 22, 2000
Evolution of chronic recurrent multifocal osteitis toward spondylarthropathy over the long term
O Vittecoq, L A Said, C Michot, et al.
European Journal of Medical Genetics
|
July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid
M Essaoui, M Nizon, M P Beaujard, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2022
SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients
M Mouillé, M Rio, S Breton, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
May 18, 2026
Characteristics and outcomes of patients with pediatric-onset non-mastocytosis mast cell activation disorders: A CEREMAST study
M Weiss, J Rossignol, F Campeotto, et al.
Clinical Genetics
|
December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome
M Nizon, M Henry, C Michot, et al.
Page
of 5