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J F Mattei

Showing results (161-170 of 202) with videos related to

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Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.
Journal De Genetique Humaine|November 1, 1976
[Rothmund's syndrome: observations in one case]A Ourgaud, H Payan, F Giraud, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndromeM A Voelckel, M C Pellissier, C Piquet, et al.
Nucleic Acids Research|March 25, 1987
Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3M Patterson, S Kenwrick, S Thibodeau, et al.
Genomics|August 1, 1989
In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15G Chimini, M G Mattei, E Passage, et al.
Genomics|August 1, 1989
Large-scale mapping and chromosome jumping in the q27 region of the human X chromosomeC Nguyen, A M Poustka, M Djabali, et al.
Human Genetics|July 1, 1986
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1A Dubart, M G Mattei, N Raich, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
Annales De Genetique|December 1, 1970
[Fertility of 45,X-46,XX and 45,X-46,XX-47,XXX women]F Giraud, M Hartung, Y Brusquet, et al.
Pageof 21

Showing results (161-170 of 202) with videos related to

Sort By:
Pageof 21
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.
Journal De Genetique Humaine|November 1, 1976
[Rothmund's syndrome: observations in one case]A Ourgaud, H Payan, F Giraud, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndromeM A Voelckel, M C Pellissier, C Piquet, et al.
Nucleic Acids Research|March 25, 1987
Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3M Patterson, S Kenwrick, S Thibodeau, et al.
Genomics|August 1, 1989
In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15G Chimini, M G Mattei, E Passage, et al.
Genomics|August 1, 1989
Large-scale mapping and chromosome jumping in the q27 region of the human X chromosomeC Nguyen, A M Poustka, M Djabali, et al.
Human Genetics|July 1, 1986
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1A Dubart, M G Mattei, N Raich, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Pediatrie|January 1, 1992
[Molecular biology in genetic counseling of Duchenne and Becker myopathy]N Philip, M A Voelckel, L Girardot, et al.
Annales De Genetique|December 1, 1970
[Fertility of 45,X-46,XX and 45,X-46,XX-47,XXX women]F Giraud, M Hartung, Y Brusquet, et al.
Pageof 21