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Human Genetics|January 1, 1979
A chromosomal abnormality (21q-) in primary thrombocytosisP Petit, H Van den BergheAllergie Et Immunologie|March 1, 1989
[Anaphylactic accidents. Etiologic and clinical study of 143 cases outside the hospital setting]E Peverelli, P Y Gueugniaud, P PetitGenetic Counseling (Geneva, Switzerland)|January 1, 1993
Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcomeP Petit, P Moerman, J P FrynsAnnales De Genetique|January 1, 1980
Silver staining of the supernumerary chromosome in the cat-eye syndromeP Petit, S Godart, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Lobar holoprosencephaly and Xq22 deletionP Petit, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter)P Petit, P Moerman, J P FrynsAmerican Journal of Medical Genetics|February 1, 1992
Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndromeP Petit, P Moerman, J P FrynsClinical Genetics|April 1, 1992
Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformationsP Petit, P Moerman, J P FrynsJournal De Radiologie|January 27, 2005
[Early cholangitis complicating percutaneous biliary drainage]V Vidal, C S Ho, P PetitBritish Journal of Rheumatology|January 1, 1992
Total knee arthroplasty infection due to Gemella haemolysansF Eggelmeijer, P Petit, B A DijkmansPageof 28