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L Larget-Piet

Showing results (31-40 of 40) with videos related to

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Journal of Pediatric Hematology/Oncology|August 1, 1996
Myelodysplastic syndrome with t(5;12)(q31;p12-p13) and eosinophilia: a pediatric case with review of literatureI Pellier, P J Le Moine, X Rialland, et al.
Journal De Genetique Humaine|January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]B Le Marec, L Larget-Piet, A Larget-Piet, et al.
Journal of Medical Genetics|September 1, 1992
Phenotype-genotype correlations in X linked retinitis pigmentosaJ Kaplan, A Pelet, C Martin, et al.
Pediatrie|June 1, 1977
[Prenatal detection of genetic diseases. Experience with 317 diagnoses]L Larget-Piet, J Berthelot, A Denis, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at riskC Lépinard, P Descamps, G Meneguzzi, et al.
American Journal of Medical Genetics|December 1, 1994
Molecular analysis of 53 fragile X families with the probe StB12.3H Puissant, M C Malinge, A Larget-Piet, et al.
Annales De Genetique|December 1, 1970
[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity]M O Rethoré, L Larget-Piet, D Abonyi, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical regionL Heidet, L Cohen-Solal, E Boye, et al.
Human Mutation|July 5, 2001
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasiaA Taillandier, A S Lia-Baldini, M Mouchard, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Journal of Pediatric Hematology/Oncology|August 1, 1996
Myelodysplastic syndrome with t(5;12)(q31;p12-p13) and eosinophilia: a pediatric case with review of literatureI Pellier, P J Le Moine, X Rialland, et al.
Journal De Genetique Humaine|January 1, 1987
[What course should be adopted after the discovery of a gonosome anomaly in the fetal karyotype?]B Le Marec, L Larget-Piet, A Larget-Piet, et al.
Journal of Medical Genetics|September 1, 1992
Phenotype-genotype correlations in X linked retinitis pigmentosaJ Kaplan, A Pelet, C Martin, et al.
Pediatrie|June 1, 1977
[Prenatal detection of genetic diseases. Experience with 317 diagnoses]L Larget-Piet, J Berthelot, A Denis, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at riskC Lépinard, P Descamps, G Meneguzzi, et al.
American Journal of Medical Genetics|December 1, 1994
Molecular analysis of 53 fragile X families with the probe StB12.3H Puissant, M C Malinge, A Larget-Piet, et al.
Annales De Genetique|December 1, 1970
[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity]M O Rethoré, L Larget-Piet, D Abonyi, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical regionL Heidet, L Cohen-Solal, E Boye, et al.
Human Mutation|July 5, 2001
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasiaA Taillandier, A S Lia-Baldini, M Mouchard, et al.
Pageof 4