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European Journal of Human Genetics : EJHG
|
July 11, 2013
A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia
B Rivera, J Perea, E Sánchez, et al.
American Journal of Medical Genetics
|
February 11, 1997
Proximal partial 5p trisomy resulting from a maternal (19;5) insertion
I Lorda-Sánchez, M Urioste, A Villa, et al.
Anales Espanoles De Pediatria
|
July 1, 1996
[The Hay-Wells syndrome, its incidence in Spain and a review of the literature]
M L Martínez-Frías, M Martín Bermejo, A Ayala Garcés, et al.
American Journal of Medical Genetics
|
September 15, 1993
Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies
M Urioste, J I Rodríguez, J M Barcia, et al.
Leukemia
|
October 6, 2001
Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas
M Renedo, B Martinez-Delgado, E Arranz, et al.
Anales Espanoles De Pediatria
|
January 1, 1988
[Familial reciprocal translocations: estimation of the most probable imbalance in the offspring]
A Díaz de Bustamante Zulueta, M A Mori Alvarez, I Pinel de la Cruz, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
October 7, 2010
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study
B Rivera, S González, E Sánchez-Tomé, et al.
Anales Espanoles De Pediatria
|
December 1, 1996
[Etiologic distribution of children with congenital defects]
M L Martínez Frías, E Rodríguez Pinilla, E Bermejo Sánchez, et al.
Sangre
|
May 24, 2000
[MLL rearrangements in acute leukemias]
M Urioste, E Arranz, B Martínez-Delgado, et al.
American Journal of Medical Genetics
|
January 1, 1994
Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome
M Urioste, G Visedo, A Sanchís, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
July 11, 2013
A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia
B Rivera, J Perea, E Sánchez, et al.
American Journal of Medical Genetics
|
February 11, 1997
Proximal partial 5p trisomy resulting from a maternal (19;5) insertion
I Lorda-Sánchez, M Urioste, A Villa, et al.
Anales Espanoles De Pediatria
|
July 1, 1996
[The Hay-Wells syndrome, its incidence in Spain and a review of the literature]
M L Martínez-Frías, M Martín Bermejo, A Ayala Garcés, et al.
American Journal of Medical Genetics
|
September 15, 1993
Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies
M Urioste, J I Rodríguez, J M Barcia, et al.
Leukemia
|
October 6, 2001
Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas
M Renedo, B Martinez-Delgado, E Arranz, et al.
Anales Espanoles De Pediatria
|
January 1, 1988
[Familial reciprocal translocations: estimation of the most probable imbalance in the offspring]
A Díaz de Bustamante Zulueta, M A Mori Alvarez, I Pinel de la Cruz, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
October 7, 2010
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study
B Rivera, S González, E Sánchez-Tomé, et al.
Anales Espanoles De Pediatria
|
December 1, 1996
[Etiologic distribution of children with congenital defects]
M L Martínez Frías, E Rodríguez Pinilla, E Bermejo Sánchez, et al.
Sangre
|
May 24, 2000
[MLL rearrangements in acute leukemias]
M Urioste, E Arranz, B Martínez-Delgado, et al.
American Journal of Medical Genetics
|
January 1, 1994
Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome
M Urioste, G Visedo, A Sanchís, et al.
Page
of 8