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American Journal of Medical Genetics
|
December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
M Smith, P A Filipek, C Wu, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2004
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation
J J Gargus, K Boyle, M Bocian, et al.
Actas Dermo-Sifiliograficas
|
May 15, 2013
Nevoid basal cell carcinoma syndrome: our experience in a pediatric hospital
P C Samela, V Tosi, A B Cervini, et al.
Actas Dermo-Sifiliograficas
|
March 17, 2012
Perianal ulcers on a segmental hemangioma with minimal or arrested growth
A Lanoel, V Tosi, M Bocian, et al.
Actas Dermo-Sifiliograficas
|
December 17, 2010
[Paraneoplastic pemphigus or paraneoplastic autoimmune multiorgan syndrome. Report of 2 cases in children and a review of the literature]
A B Cervini, V Tosi, S H Kim, et al.
Cell
|
July 29, 1994
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
R Shiang, L M Thompson, Y Z Zhu, et al.
American Journal of Medical Genetics
|
August 1, 1986
Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunk
C O Reid, J G Hall, C Anderson, et al.
Frontiers in Microbiology
|
August 11, 2016
Engineering of Helicobacter pylori Dimeric Oxidoreductase DsbK (HP0231)
Katarzyna M Bocian-Ostrzycka, Magdalena J Grzeszczuk, Anna M Banaś, et al.
International Journal of Medical Microbiology : IJMM
|
August 23, 2018
Thioloxidoreductase HP0231 of Helicobacter pylori impacts HopQ-dependent CagA translocation
Magdalena J Grzeszczuk, Katarzyna M Bocian-Ostrzycka, Anna M Banaś, et al.
American Journal of Medical Genetics
|
June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II
H J Stern, J M Graham, R S Lachman, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
December 20, 2000
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
M Smith, P A Filipek, C Wu, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2004
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation
J J Gargus, K Boyle, M Bocian, et al.
Actas Dermo-Sifiliograficas
|
May 15, 2013
Nevoid basal cell carcinoma syndrome: our experience in a pediatric hospital
P C Samela, V Tosi, A B Cervini, et al.
Actas Dermo-Sifiliograficas
|
March 17, 2012
Perianal ulcers on a segmental hemangioma with minimal or arrested growth
A Lanoel, V Tosi, M Bocian, et al.
Actas Dermo-Sifiliograficas
|
December 17, 2010
[Paraneoplastic pemphigus or paraneoplastic autoimmune multiorgan syndrome. Report of 2 cases in children and a review of the literature]
A B Cervini, V Tosi, S H Kim, et al.
Cell
|
July 29, 1994
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
R Shiang, L M Thompson, Y Z Zhu, et al.
American Journal of Medical Genetics
|
August 1, 1986
Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunk
C O Reid, J G Hall, C Anderson, et al.
Frontiers in Microbiology
|
August 11, 2016
Engineering of Helicobacter pylori Dimeric Oxidoreductase DsbK (HP0231)
Katarzyna M Bocian-Ostrzycka, Magdalena J Grzeszczuk, Anna M Banaś, et al.
International Journal of Medical Microbiology : IJMM
|
August 23, 2018
Thioloxidoreductase HP0231 of Helicobacter pylori impacts HopQ-dependent CagA translocation
Magdalena J Grzeszczuk, Katarzyna M Bocian-Ostrzycka, Anna M Banaś, et al.
American Journal of Medical Genetics
|
June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II
H J Stern, J M Graham, R S Lachman, et al.
Page
of 4