Publications by authors named "Peter Mo"

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Towards a content agnostic computable knowledge repository for data quality assessment.
Naresh Sundar Rajan, Ramkiran Gouripeddi, Peter Mo, Randy K Madsen, Julio C Facelli

Comput Methods Programs Biomed· August 2019

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Federating clinical data from six pediatric hospitals: process and initial results for microbiology from the PHIS+ consortium.
Ramkiran Gouripeddi, Phillip B Warner, Peter Mo, James E Levin, Rajendu Srivastava

AMIA Annu Symp Proc· July 2013

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Federating clinical data from six pediatric hospitals: process and initial results from the PHIS+ Consortium.
Scott P Narus, Rajendu Srivastava, Ramkiran Gouripeddi, Oren E Livne, Peter Mo

AMIA Annu Symp Proc· February 2013

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[Involvement of thyroid gland at non-Hodgkin lymphoma initial diagnosis: 2 pediatric cases].
S Frache, M O Peter, V Laithier, A M Bertrand, G Thiriez

Arch Pediatr· January 2006

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Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome.
Houda Karmous-Benailly, Jelena Martinovic, Marie-Claire Gubler, Yoann Sirot, Laure Clech, Brigitte Simon-Bouy

Am J Hum Genet· March 2005

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Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12.
Clotilde Lagier-Tourenne, E Ginglinger, Y Alembik, A De Saint Martin, M O Peter

Am J Med Genet A· February 2004

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Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia.
G Lina, Y Piémont, F Godail-Gamot, M Bes, M O Peter

Clin Infect Dis· November 1999

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Familial association of camptodactyly, mental retardation, whistling face and Pierre Robin sequence.
C Stoll, F Benoit, M O Peter, B Gasser

Clin Dysmorphol· October 1999

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Evaluation of prenatal diagnosis of congenital heart disease.
C Stoll, Y Alembik, B Dott, M J Meyer, A Pennerath

Prenat Diagn· August 1998

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[Superior sagittal sinus thrombosis and nephrotic syndrome: favorable outcome with low molecular weight heparin].
A de Saint-Martin, J Terzic, D Christmann, M C Knab, M O Peter

Arch Pediatr· September 1997

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Brachytelephalangic chondrodysplasia punctata in a female child.
M O Peter, E Jeandidier, P Maroteaux

J Pediatr Orthop B· January 1997

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Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.
A Sefiani, R M'rad, L Simard, A Vincent, C Julier

Hum Genet· January 1991

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Distal trisomy 14q. I. Clinical and cytogenetical studies.
S Gilgenkrantz, J Vigneron, M O Peter, J L Dufier, M Teboul

Hum Genet· October 1990

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[Lethal syndromes with thin bones].
P Maroteaux, L Cohen-Solal, J Bonaventure, M O Peter, C Francannet, C Moraine

Arch Fr Pediatr· January 1989

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Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
A Sefiani, D Sinnett, L Abel, S Szpiro-Tapia, S Heuertz

Hum Genet· November 1988

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Early prenatal diagnosis of inherited severe immunodeficiencies linked to enzyme deficiencies.
J L Pérignon, A Durandy, M O Peter, F Freycon, Y Dumez

J Pediatr· October 1987

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[Neonatal form of isovaleric acidemia. Apropos of a new case].
P Beauvais, M O Peter, B Barbier

Arch Fr Pediatr· February 1986

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[Gyrate atrophy of the choroid and retina in children. Apropos of 2 cases].
M O Peter, J Klethi, G Payeur, M J Meyer, P Beauvais

Pediatrie· March 1984

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[Physiological variations of serum complement in children].
J Geisert, R Sacrez, J Malgras, G Hauptmann, M O Peter

Pediatrie· September 1971

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[Blood insulin in normal newborn infants during provoked hyperglycemia by the intravenous route].
J M Levy, N Segura, F Klein, C Grunewald, R Thierry

Arch Fr Pediatr· February 1971

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