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M A Alliende

Showing results (1-10 of 9) with videos related to

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Revista Chilena De Pediatria|September 1, 1982
[The differential diagnosis of syndromes of bone marrow hypoplasia associated with malformation of the extremities]B Curotto, M A Alliende, Y Lacassie
Revista Medica De Chile|June 21, 2001
[Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis]L Santa María, B Curotto, F Cortés, et al.
Revista Medica De Chile|May 1, 1984
[Preliminary evaluation of the treatment with folic acid in 2 patients with sex-linked mental retardation and macroorchidism]Y Lacassie, B Curotto, M A Alliende, et al.
Revista Medica De Chile|June 1, 1999
[Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families]M A Alliende, B Urzúa, A Valiente, et al.
Revista Chilena De Pediatria|September 1, 1982
[Phenotypic screening for X-linked mental retardation: fragile Xq syndrome]I Lacassie, A B Zavala, B Curotto, et al.
Revista Chilena De Pediatria|March 1, 1986
[Trisomy 22]E Raimann, M A Alliende, M V Carvajal, et al.
Revista Chilena De Pediatria|November 1, 1986
[Ambiguous sex with a 45,X/45,X,t(Y;14) chromosomal constitution]C Noziglia, M A Alliende, M V Carvajal, et al.
Neurologia (Barcelona, Spain)|December 23, 2014
Clinical, molecular, and pharmacological aspects of FMR1 related disordersA Pugin, V Faundes, L Santa María, et al.
Clinical Genetics|September 14, 2013
FXTAS in an unmethylated mosaic male with fragile X syndrome from ChileL Santa María, A Pugin, M A Alliende, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Revista Chilena De Pediatria|September 1, 1982
[The differential diagnosis of syndromes of bone marrow hypoplasia associated with malformation of the extremities]B Curotto, M A Alliende, Y Lacassie
Revista Medica De Chile|June 21, 2001
[Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis]L Santa María, B Curotto, F Cortés, et al.
Revista Medica De Chile|May 1, 1984
[Preliminary evaluation of the treatment with folic acid in 2 patients with sex-linked mental retardation and macroorchidism]Y Lacassie, B Curotto, M A Alliende, et al.
Revista Medica De Chile|June 1, 1999
[Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families]M A Alliende, B Urzúa, A Valiente, et al.
Revista Chilena De Pediatria|September 1, 1982
[Phenotypic screening for X-linked mental retardation: fragile Xq syndrome]I Lacassie, A B Zavala, B Curotto, et al.
Revista Chilena De Pediatria|March 1, 1986
[Trisomy 22]E Raimann, M A Alliende, M V Carvajal, et al.
Revista Chilena De Pediatria|November 1, 1986
[Ambiguous sex with a 45,X/45,X,t(Y;14) chromosomal constitution]C Noziglia, M A Alliende, M V Carvajal, et al.
Neurologia (Barcelona, Spain)|December 23, 2014
Clinical, molecular, and pharmacological aspects of FMR1 related disordersA Pugin, V Faundes, L Santa María, et al.
Clinical Genetics|September 14, 2013
FXTAS in an unmethylated mosaic male with fragile X syndrome from ChileL Santa María, A Pugin, M A Alliende, et al.
Pageof 1