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J FREZAL

Showing results (31-40 of 61) with videos related to

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Bulletin Des Societes D'Ophtalmologie De France|October 1, 1988
[Detection of genetic carriers and antenatal diagnosis of juvenile retinoschisis by familial analysis in molecular biology]J Kaplan, A Pelet, A Munnich, et al.
Archives Francaises De Pediatrie|February 1, 1975
[Frequency of birth defects. Study of a maternity hospital in Paris]M L Briard, J Feingold, C Bonaiti-Pellie, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Annales De Genetique|December 1, 1975
[Prevalence of etinoblastoma in the Midi-Pyrenées area]C Bonaiti-Pellie, P Colombies, P Bec, et al.
Lancet (London, England)|May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiencyA Munnich, J M Saudubray, F X Coude, et al.
Lancet (London, England)|April 10, 1982
Antenatal diagnosis of severe combined immunodeficiency from fetal cord bloodA Durandy, C Griscelli, Y Dumez, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|June 1, 1989
[Associated forms of hereditary chorioretinal degeneration]N Manderieux, J L Dufier, J Kaplan, et al.
Archives Francaises De Pediatrie|August 1, 1985
[Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form]J P Bonnefont, H Ogier, G Mitchell, et al.
Annales De Genetique|January 1, 1990
Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneityJ Kaplan, G Guasconi, J L Dufier, et al.
The Journal of Pediatrics|June 1, 1984
Congenital anomalies in glutaric aciduria type 2G Mitchell, J M Saudubray, M C Gubler, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

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Pageof 7
Bulletin Des Societes D'Ophtalmologie De France|October 1, 1988
[Detection of genetic carriers and antenatal diagnosis of juvenile retinoschisis by familial analysis in molecular biology]J Kaplan, A Pelet, A Munnich, et al.
Archives Francaises De Pediatrie|February 1, 1975
[Frequency of birth defects. Study of a maternity hospital in Paris]M L Briard, J Feingold, C Bonaiti-Pellie, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Annales De Genetique|December 1, 1975
[Prevalence of etinoblastoma in the Midi-Pyrenées area]C Bonaiti-Pellie, P Colombies, P Bec, et al.
Lancet (London, England)|May 17, 1980
Fatty-acid-responsive alopecia in multiple carboxylase deficiencyA Munnich, J M Saudubray, F X Coude, et al.
Lancet (London, England)|April 10, 1982
Antenatal diagnosis of severe combined immunodeficiency from fetal cord bloodA Durandy, C Griscelli, Y Dumez, et al.
Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|June 1, 1989
[Associated forms of hereditary chorioretinal degeneration]N Manderieux, J L Dufier, J Kaplan, et al.
Archives Francaises De Pediatrie|August 1, 1985
[Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form]J P Bonnefont, H Ogier, G Mitchell, et al.
Annales De Genetique|January 1, 1990
Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneityJ Kaplan, G Guasconi, J L Dufier, et al.
The Journal of Pediatrics|June 1, 1984
Congenital anomalies in glutaric aciduria type 2G Mitchell, J M Saudubray, M C Gubler, et al.
Pageof 7