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J Gabarrón

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European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in SpainJ Gabarrón, C Ramos
Cytogenetics and Cell Genetics|January 1, 1986
Premature centromere division dominantly inherited in a subfertile familyJ Gabarrón, A Jimenez, G Glover
American Journal of Medical Genetics|April 1, 1992
Fragile X screening program in a Spanish regionJ Gabarrón, I Lopez, G Glover, et al.
Human Genetics|June 1, 1987
De novo 10q(q21q22) interstitial deletionG Glover, J Gabarrón, J A López Ballester
Clinical Genetics|December 1, 1985
Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter----q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and "cat eye" phenotypical featuresJ Gabarrón, G Glover, A Jimenez, et al.
Clinical Genetics|April 1, 1988
Partial monosomy 6q(q15q21) by de novo interstitial deletionG Glover, I López, J Gabarrón, et al.
Clinical Genetics|March 1, 1988
Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotypeJ Gabarrón, G Glover, A Jiménez, et al.
American Journal of Medical Genetics|August 9, 1996
FRAXE mutation analysis in three Spanish familiesP Carbonell, I López, J Gabarrón, et al.
Anales Espanoles De Pediatria|October 1, 1984
[Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families]T Rodríguez Costa, J Gabarrón Llamas, C Casas Fernández, et al.
Anales Espanoles De Pediatria|December 1, 1981
["De novo" partial trisomy 16p (author's transl)]J Gabarrón Llamas, D Cabrerizo Portero, F Montserrat Bernal, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in SpainJ Gabarrón, C Ramos
Cytogenetics and Cell Genetics|January 1, 1986
Premature centromere division dominantly inherited in a subfertile familyJ Gabarrón, A Jimenez, G Glover
American Journal of Medical Genetics|April 1, 1992
Fragile X screening program in a Spanish regionJ Gabarrón, I Lopez, G Glover, et al.
Human Genetics|June 1, 1987
De novo 10q(q21q22) interstitial deletionG Glover, J Gabarrón, J A López Ballester
Clinical Genetics|December 1, 1985
Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter----q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and "cat eye" phenotypical featuresJ Gabarrón, G Glover, A Jimenez, et al.
Clinical Genetics|April 1, 1988
Partial monosomy 6q(q15q21) by de novo interstitial deletionG Glover, I López, J Gabarrón, et al.
Clinical Genetics|March 1, 1988
Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotypeJ Gabarrón, G Glover, A Jiménez, et al.
American Journal of Medical Genetics|August 9, 1996
FRAXE mutation analysis in three Spanish familiesP Carbonell, I López, J Gabarrón, et al.
Anales Espanoles De Pediatria|October 1, 1984
[Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families]T Rodríguez Costa, J Gabarrón Llamas, C Casas Fernández, et al.
Anales Espanoles De Pediatria|December 1, 1981
["De novo" partial trisomy 16p (author's transl)]J Gabarrón Llamas, D Cabrerizo Portero, F Montserrat Bernal, et al.
Pageof 2