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M Lerone

Showing results (51-60 of 70) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Pediatric Radiology|January 1, 1991
Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvementM Lerone, P Dodero, G Romeo, et al.
Minerva Medica|March 24, 1981
[Frequency of microcythemias in the provinces of Latium]E Silvestroni, I Bianco, B Graziani, et al.
Journal of Medical Genetics|July 7, 2000
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervationM Costa, M Fava, M Seri, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Haematologica|May 1, 1997
Silent thalassemias: genotypes and phenotypesI Bianco, M P Cappabianca, E Foglietta, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Journal of Medical Genetics|September 10, 2003
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's diseaseM Sancandi, P Griseri, B Pesce, et al.
Acta Haematologica|January 1, 1984
A study of the mechanisms and sites of action of desferrioxamine in thalassaemia majorI Bianco, B Graziani, M Lerone, et al.
Bone|May 28, 2021
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruptionE Tassano, P Ronchetto, M Severino, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|January 1, 1994
Heterogeneity and low detection rate of RET mutations in Hirschsprung diseaseL Yin, V Barone, M Seri, et al.
Pediatric Radiology|January 1, 1991
Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvementM Lerone, P Dodero, G Romeo, et al.
Minerva Medica|March 24, 1981
[Frequency of microcythemias in the provinces of Latium]E Silvestroni, I Bianco, B Graziani, et al.
Journal of Medical Genetics|July 7, 2000
Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervationM Costa, M Fava, M Seri, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Haematologica|May 1, 1997
Silent thalassemias: genotypes and phenotypesI Bianco, M P Cappabianca, E Foglietta, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Journal of Medical Genetics|September 10, 2003
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's diseaseM Sancandi, P Griseri, B Pesce, et al.
Acta Haematologica|January 1, 1984
A study of the mechanisms and sites of action of desferrioxamine in thalassaemia majorI Bianco, B Graziani, M Lerone, et al.
Bone|May 28, 2021
Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruptionE Tassano, P Ronchetto, M Severino, et al.
Pageof 7