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American Journal of Medical Genetics. Part A
|
August 15, 2006
Array comparative genomic hybridization analysis in first-trimester spontaneous abortions with 'normal' karyotypes
Osamu Shimokawa, Naoki Harada, Noriko Miyake, et al.
International Medical Case Reports Journal
|
April 3, 2023
Platypnea-Orthodeoxia Syndrome in Coronavirus Disease 2019 Pneumonia: A Case Report and Literature Review
Takahiko Tanimoto, Yoshihiro Eriguchi, Tomonori Sato, et al.
Infection and Drug Resistance
|
July 20, 2017
Incomplete recovery of the fecal flora of hematological patients with neutropenia and repeated fluoroquinolone prophylaxis
Yong Chong, Shinji Shimoda, Noriko Miyake, et al.
Journal of Human Genetics
|
October 17, 2014
Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly
Hirotomo Saitsu, Sumimasa Yamashita, Yukichi Tanaka, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
April 23, 2010
[Serum zinc concentration decreases with age and is associated with anemia in middle-aged and elderly people]
Mayumi Idei, Kazunori Miyake, Yuki Horiuchi, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Paternal somatic mosaicism of a TGFBR2 mutation transmitting to an affected son with Loeys-Dietz syndrome
Yoriko Watanabe, Haruya Sakai, Akira Nishimura, et al.
Journal of Human Genetics
|
April 17, 2019
Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome
Ming Lei, Satomi Mitsuhashi, Noriko Miyake, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
July 17, 2024
Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle
Shigemi Kimura, Noriko Miyake, Shiro Ozasa, et al.
American Journal of Medical Genetics. Part A
|
March 7, 2013
A de novo deletion at 16q24.3 involving ANKRD11 in a Japanese patient with KBG syndrome
Satoko Miyatake, Akira Murakami, Nobuhiko Okamoto, et al.
The Journal of Nutrition
|
October 9, 2002
Phytoestrogen concentrations in serum from Japanese men and women over forty years of age
Michael S Morton, Osamu Arisaka, Noriko Miyake, et al.
Page
of 47
Search research articles
Search
Showing results (51-60 of 463) with videos related to
Sort By:
Page
of 47
American Journal of Medical Genetics. Part A
|
August 15, 2006
Array comparative genomic hybridization analysis in first-trimester spontaneous abortions with 'normal' karyotypes
Osamu Shimokawa, Naoki Harada, Noriko Miyake, et al.
International Medical Case Reports Journal
|
April 3, 2023
Platypnea-Orthodeoxia Syndrome in Coronavirus Disease 2019 Pneumonia: A Case Report and Literature Review
Takahiko Tanimoto, Yoshihiro Eriguchi, Tomonori Sato, et al.
Infection and Drug Resistance
|
July 20, 2017
Incomplete recovery of the fecal flora of hematological patients with neutropenia and repeated fluoroquinolone prophylaxis
Yong Chong, Shinji Shimoda, Noriko Miyake, et al.
Journal of Human Genetics
|
October 17, 2014
Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly
Hirotomo Saitsu, Sumimasa Yamashita, Yukichi Tanaka, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
April 23, 2010
[Serum zinc concentration decreases with age and is associated with anemia in middle-aged and elderly people]
Mayumi Idei, Kazunori Miyake, Yuki Horiuchi, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Paternal somatic mosaicism of a TGFBR2 mutation transmitting to an affected son with Loeys-Dietz syndrome
Yoriko Watanabe, Haruya Sakai, Akira Nishimura, et al.
Journal of Human Genetics
|
April 17, 2019
Translocation breakpoint disrupting the host SNHG14 gene but not coding genes or snoRNAs in typical Prader-Willi syndrome
Ming Lei, Satomi Mitsuhashi, Noriko Miyake, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
July 17, 2024
Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle
Shigemi Kimura, Noriko Miyake, Shiro Ozasa, et al.
American Journal of Medical Genetics. Part A
|
March 7, 2013
A de novo deletion at 16q24.3 involving ANKRD11 in a Japanese patient with KBG syndrome
Satoko Miyatake, Akira Murakami, Nobuhiko Okamoto, et al.
The Journal of Nutrition
|
October 9, 2002
Phytoestrogen concentrations in serum from Japanese men and women over forty years of age
Michael S Morton, Osamu Arisaka, Noriko Miyake, et al.
Page
of 47