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1دورية أكاديمية
المؤلفون: Van Khanh Tran, My Ha Cao, Thi Thanh Hai Nguyen, Phuong Thi Le, Hai Anh Tran, Dung Chi Vu, Ha Thu Nguyen, Mai Thi Phương Nguyen, The-Hung Bui, Thanh Binh Nguyen, Thanh Van Ta, Thinh Huy Tran
المصدر: Frontiers in Pediatrics, Vol 12 (2024)
مصطلحات موضوعية: IGHMBP2, neuromuscular disorders, SMARD1, CMT2S, Charcot–Marie–Tooth type 2S, spinal muscular atrophy with respiratory distress type 1, Pediatrics, RJ1-570
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Thinh Huy Tran, Quang Minh Diep, My Ha Cao, Long Hoang Luong, Van Anh Pham, Oanh Thi Lan Dinh, The-Hung Bui, Thanh Van Ta, Van Khanh Tran
المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 5, Pp 907-910 (2021)
مصطلحات موضوعية: Microcephaly primary hereditary, ASPM, MCPH5, Exome sequencing, Gynecology and obstetrics, RG1-991
وصف الملف: electronic resource
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3
المؤلفون: Oanh Thi Lan Dinh, Thanh Van Ta, Thinh Huy Tran, The-Hung Bui, My Ha Cao, Long Hoang Luong, Quang Minh Diep, Van Anh Pham, Van Khanh Tran
المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 5, Pp 907-910 (2021)
مصطلحات موضوعية: Adult, Exome sequencing, Microcephaly, Pediatrics, medicine.medical_specialty, Genetic counseling, ASPM, Nerve Tissue Proteins, Prenatal diagnosis, Compound heterozygosity, Asian People, Pregnancy, Intellectual Disability, Prenatal Diagnosis, Intellectual disability, medicine, Humans, Child, Microcephaly primary hereditary, Genetic testing, medicine.diagnostic_test, business.industry, Infant, Newborn, Obstetrics and Gynecology, Gynecology and obstetrics, medicine.disease, Vietnam, MCPH5, Mutation, RG1-991, Female, business
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4
المؤلفون: Van Khanh Tran, Thinh Huy Tran, Thanh Van Ta, Duc Hinh Nguyen, Dung Chi Vu, Thanh Dat Ta, My Ha Cao, The-Hung Bui, Phuong Thi Le, Long Hoang Luong
المصدر: American Journal of Medical Genetics Part A.
مصطلحات موضوعية: Adult, Male, Heterozygote, medicine.drug_class, DNA Mutational Analysis, Gene Expression, Disease, Compound heterozygosity, Short stature, Bone and Bones, Skeletal disorder, Genetics, Natriuretic peptide, Humans, Medicine, Genetic Testing, Child, Genetics (clinical), Bone Diseases, Developmental, business.industry, Homozygote, NPR2, Pedigree, Radiography, Phenotype, Vietnam, Child, Preschool, Mutation, Female, Acromesomelic dysplasia Maroteaux type, medicine.symptom, business, Receptors, Atrial Natriuretic Factor, Rare disease
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5دورية أكاديمية
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