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E Mornet

Showing results (21-30 of 86) with videos related to

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Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
Immunogenetics|January 1, 1988
Extensive genomic polymorphism in mouse 21-hydroxylase regionD Gillet, E Mornet, A Rocca, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
General cystic fibrosis mutations are usually missense mutations affecting two specific protein domains and associated with a specific RFLP marker haplotypeJ L Serre, E Mornet, B Simon-Bouy, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|June 4, 2013
Vestibular schwannoma and cell-phones. Results, limits and perspectives of clinical studiesE Mornet, R Kania, E Sauvaget, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|October 31, 2013
Outpatient hemithyroidectomyC Lacroix, G Potard, C Clodic, et al.
Archives Francaises De Pediatrie|March 1, 1985
[Congenital adrenal hyperplasia (21-OH) in France. Population genetics]E Bois, E Mornet, A Chompret, et al.
Clinical Genetics|January 15, 2000
Perinatal hypophosphatasia: diagnosis and detection of heterozygote carriers within the familyB Gehring, E Mornet, H Plath, et al.
Journal of Medical Genetics|January 1, 1994
Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndromeM I Tejada, E Mornet, E Tizzano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 17, 2002
Hypophosphatasia associated with increased nuchal translucency: a report of two affected pregnanciesA P Souka, F L Raymond, E Mornet, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) geneC Stoll, M Fischbach, J Terzic, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
Immunogenetics|January 1, 1988
Extensive genomic polymorphism in mouse 21-hydroxylase regionD Gillet, E Mornet, A Rocca, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
General cystic fibrosis mutations are usually missense mutations affecting two specific protein domains and associated with a specific RFLP marker haplotypeJ L Serre, E Mornet, B Simon-Bouy, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|June 4, 2013
Vestibular schwannoma and cell-phones. Results, limits and perspectives of clinical studiesE Mornet, R Kania, E Sauvaget, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|October 31, 2013
Outpatient hemithyroidectomyC Lacroix, G Potard, C Clodic, et al.
Archives Francaises De Pediatrie|March 1, 1985
[Congenital adrenal hyperplasia (21-OH) in France. Population genetics]E Bois, E Mornet, A Chompret, et al.
Clinical Genetics|January 15, 2000
Perinatal hypophosphatasia: diagnosis and detection of heterozygote carriers within the familyB Gehring, E Mornet, H Plath, et al.
Journal of Medical Genetics|January 1, 1994
Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndromeM I Tejada, E Mornet, E Tizzano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 17, 2002
Hypophosphatasia associated with increased nuchal translucency: a report of two affected pregnanciesA P Souka, F L Raymond, E Mornet, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Severe hypophosphatasia due to mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) geneC Stoll, M Fischbach, J Terzic, et al.
Pageof 9