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1Academic Journal
المؤلفون: Kazuko MARUO, Makoto MINO, Mie IWAKOSHI, Shigeo NAKAGAWA, Toshiko HIMEDA, 中川 茂男, 丸尾 和子, 姫田 淑子, 岩越 美恵, 美濃 真
المصدر: ビタミン / VITAMINS. 1980, 54(3):95
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2Academic Journal
المؤلفون: Eiji WAKAMIYA, Hiroshi TAMAI, Makoto MINO, Mie IWAKOSHI
المصدر: Journal of Nutritional Science and Vitaminology. 1988, 34(6):627
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3Academic Journal
المؤلفون: Makoto MINO, Mie IWAKOSHI, Shigeo NAKAGAWA, Yasuhiko NISHIDA, Yoshitami KIJIMA
المصدر: Journal of Nutritional Science and Vitaminology. 1979, 25(6):505
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4Academic Journal
المؤلفون: Makoto MINO, Mie IWAKOSHI, Shigeo NAKAGAWA, Yasuhiko NISHIDA
المصدر: Journal of Nutritional Science and Vitaminology. 1982, 28(3):237
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5
المؤلفون: Kazunori Ohama, Mitsuharu Kajita, Kenichiro Yamada, Naoko Ishihara, Mie Iwakoshi, Kenji Kurosawa, Kiyokuni Miura, Daisuke Fukushi, Yayoi Fukuhara, Kenjiro Kosaki, Reiko Kimura, Eriko Nishi, Yuto Yamamoto, Tatsuo Kuroda, Mari Matsuo, Kiyoko Sameshima, Akira Ohta, Nobuhiko Okamoto, Seiji Mizuno, Rika Kosaki, Kenji Yokochi, Shin ichiro Hamano, Hiroshi Suzumura, Yasukazu Yamada, Nobuaki Wakamatsu, Hiroyuki Wakamoto, Kayoko Saito, George Imataka, Yuka Suzuki, Yoko Hiraki, Noriko Nomura, Kenji Shimizu
المصدر: American Journal of Medical Genetics Part A. 164:1899-1908
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Microcephaly, Adolescent, Mowat–Wilson syndrome, media_common.quotation_subject, Nonsense mutation, Nonsense, Gene Expression, Biology, medicine.disease_cause, Cell Line, Frameshift mutation, Young Adult, Japan, Intellectual Disability, Prevalence, Genetics, medicine, Humans, Hirschsprung Disease, RNA, Messenger, Allele, Child, Frameshift Mutation, Alleles, Genetic Association Studies, Genetics (clinical), Zinc Finger E-box Binding Homeobox 2, media_common, Homeodomain Proteins, Mutation, Protein Stability, Facies, Infant, medicine.disease, Hypoplasia, Repressor Proteins, Phenotype, Codon, Nonsense, Child, Preschool, Female
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6
المؤلفون: Naoki Harada, Nobuhiko Okamoto, Shunji Yamamori, Hiroko Fujita, Naomichi Matsumoto, Norio Niikawa, Mie Iwakoshi, Tsuyoshi Nakamura
المصدر: American Journal of Medical Genetics. :278-283
مصطلحات موضوعية: Heart Defects, Congenital, Male, Microcephaly, medicine.medical_specialty, Monosomy, Adolescent, Limb Deformities, Congenital, Chromosome Disorders, Trisomy, Biology, Translocation, Genetic, Protruding tongue, Intellectual Disability, Internal medicine, medicine, Humans, Abnormalities, Multiple, Hypertelorism, Child, Genetics (clinical), Kleefstra Syndrome, Chromosomes, Human, 6-12 and X, Pointed chin, Infant, Newborn, Syndrome, medicine.disease, Dermatology, Endocrinology, Hypospadias, Child, Preschool, Face, Karyotyping, Female, Chromosome Deletion, medicine.symptom, Chromosomes, Human, Pair 9
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7
المؤلفون: Norio Niikawa, Tohru Ohta, Naoki Harada, Osamu Shimokawa, Haruya Sakai, Noriko Miyake, Hirotomo Saitsu, Shinji Saitoh, Naomichi Matsumoto, Kanako Sato, Mie Iwakoshi, Takeshi Mizuguchi
المصدر: American journal of medical genetics. Part A. (1)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Chromosomes, Human, Pair 15, Base Sequence, DNA Mutational Analysis, Personalized health, medicine.disease, Pedigree, Phenotype, Angelman syndrome, Family medicine, Child, Preschool, Happy puppet syndrome, Genetics, medicine, Humans, Female, Congenital disease, Angelman Syndrome, Chromosome Deletion, Medical science, Psychology, Genetics (clinical), In Situ Hybridization, Fluorescence
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8
المؤلفون: Tohru Ohta, Yoshio Makita, Ko Ichiro Yoshiura, Osamu Shimokawa, Aiko Okubo, Nobuhiko Okamoto, Noriko Miyake, Mie Iwakoshi, Norio Niikawa, Hiroki Kawara, Yoko Hiraki, Naomichi Matsumoto, Tatsuya Kishino, Nadia Sosonkina, Masayo Nomura, Naoki Harada, Hiroshi Kawame, Takeshi Mizuguchi, Yoshimitsu Fukushima, Tomoki Kosho, Mitsuhiro Kato, Yuji Yokoyama, Kenji Kurosawa, Takanori Yamagata
المصدر: American journal of medical genetics. Part A. 140(3)
مصطلحات موضوعية: Male, Chromosomes, Artificial, Bacterial, Genomics, Chromosomal translocation, Biology, Translocation, Genetic, Intellectual Disability, Chromosomal Abnormality, Gene duplication, Genetics, medicine, Humans, Genetics (clinical), In Situ Hybridization, Fluorescence, Chromosome Aberrations, medicine.diagnostic_test, Genome, Human, Fish analysis, Nucleic Acid Hybridization, Chromosome Banding, Karyotyping, Human genome, Female, Chromosome Deletion, Fluorescence in situ hybridization, Comparative genomic hybridization
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9
المؤلفون: Nobuhiko Okamoto, Tatsuya Kishino, Naoki Harada, Remco Visser, Naomichi Matsumoto, Norio Niikawa, Makoto Fukamachi, Angie Dawson, Mie Iwakoshi
المصدر: Journal of human genetics. 49(8)
مصطلحات موضوعية: Male, Microcephaly, Candidate gene, Chromosomes, Artificial, Bacterial, Centromere, Chromosome Disorders, Biology, Protruding tongue, Intellectual Disability, Genetics, medicine, Humans, Hypertelorism, Genetics (clinical), In Situ Hybridization, Fluorescence, medicine.diagnostic_test, Haplotype, Syndrome, Telomere, medicine.disease, Phenotype, Hypotonia, Haplotypes, Female, medicine.symptom, Chromosome Deletion, Chromosomes, Human, Pair 9, Fluorescence in situ hybridization
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10
المؤلفون: Mie Iwakoshi, Yasuhiko Nishida, Shigeo Nakagawa, Yoshitami Kijima, Makoto Mino
المصدر: Journal of nutritional science and vitaminology. 25(6)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Aging, Erythrocytes, Adolescent, Medicine (miscellaneous), gamma-Tocopherol, Alpha (ethology), chemistry.chemical_compound, Pregnancy, Internal medicine, medicine, Humans, Vitamin E, heterocyclic compounds, Tocopherol, Child, Chromatography, High Pressure Liquid, Nutrition and Dietetics, Human blood, Chemistry, Erythrocyte Membrane, Infant, Newborn, food and beverages, Infant, hemic and immune systems, Plasma levels, Fetal Blood, Red blood cell, Endocrinology, medicine.anatomical_structure, Cord blood, Child, Preschool, Immunology, lipids (amino acids, peptides, and proteins), Female, alpha-Tocopherol, Infant, Premature, circulatory and respiratory physiology
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