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American Journal of Medical Genetics. Part A
|
May 14, 2014
Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion
Francesca Novara, Franco Stanzial, Elena Rossi, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Periventricular nodular heterotopia in Smith-Magenis syndrome
Valeria Capra, Roberta Biancheri, Giovanni Morana, et al.
Journal of Human Genetics
|
October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinoma
Ivan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
Human Mutation
|
April 18, 2012
The introduction of arrays in prenatal diagnosis: a special challenge
Annalisa Vetro, Katelijne Bouman, Ros Hastings, et al.
Cancer Research
|
October 3, 2007
Human bone marrow derived mesenchymal stem cells do not undergo transformation after long-term in vitro culture and do not exhibit telomere maintenance mechanisms
Maria Ester Bernardo, Nadia Zaffaroni, Francesca Novara, et al.
European Journal of Medical Genetics
|
February 14, 2013
MEF2C deletions and mutations versus duplications: a clinical comparison
Francesca Novara, Ambra Rizzo, Gloria Bedini, et al.
Molecular Cytogenetics
|
November 2, 2013
Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH
Emmanouil Manolakos, Konstantinos Kefalas, Annalisa Vetro, et al.
European Journal of Human Genetics : EJHG
|
July 22, 2004
Inverted duplications: how many of them are mosaic?
Tiziano Pramparo, Sabrina Giglio, Giuliana Gregato, et al.
Human Genetics
|
July 26, 2005
Reciprocal translocations: a trap for cytogenetists?
Roberto Ciccone, Roberto Giorda, Giuliana Gregato, et al.
Journal of Translational Medicine
|
April 11, 2014
In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients
Enrico Lucarelli, Chiara Bellotti, Melissa Mantelli, et al.
Page
of 23
Search research articles
Search
Showing results (131-140 of 222) with videos related to
Sort By:
Page
of 23
American Journal of Medical Genetics. Part A
|
May 14, 2014
Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion
Francesca Novara, Franco Stanzial, Elena Rossi, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Periventricular nodular heterotopia in Smith-Magenis syndrome
Valeria Capra, Roberta Biancheri, Giovanni Morana, et al.
Journal of Human Genetics
|
October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinoma
Ivan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
Human Mutation
|
April 18, 2012
The introduction of arrays in prenatal diagnosis: a special challenge
Annalisa Vetro, Katelijne Bouman, Ros Hastings, et al.
Cancer Research
|
October 3, 2007
Human bone marrow derived mesenchymal stem cells do not undergo transformation after long-term in vitro culture and do not exhibit telomere maintenance mechanisms
Maria Ester Bernardo, Nadia Zaffaroni, Francesca Novara, et al.
European Journal of Medical Genetics
|
February 14, 2013
MEF2C deletions and mutations versus duplications: a clinical comparison
Francesca Novara, Ambra Rizzo, Gloria Bedini, et al.
Molecular Cytogenetics
|
November 2, 2013
Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH
Emmanouil Manolakos, Konstantinos Kefalas, Annalisa Vetro, et al.
European Journal of Human Genetics : EJHG
|
July 22, 2004
Inverted duplications: how many of them are mosaic?
Tiziano Pramparo, Sabrina Giglio, Giuliana Gregato, et al.
Human Genetics
|
July 26, 2005
Reciprocal translocations: a trap for cytogenetists?
Roberto Ciccone, Roberto Giorda, Giuliana Gregato, et al.
Journal of Translational Medicine
|
April 11, 2014
In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients
Enrico Lucarelli, Chiara Bellotti, Melissa Mantelli, et al.
Page
of 23