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المؤلفون: Saima Mustafa, Malik Fiaz Hussain, Muhammad Latif, Maryam Ijaz, Muhammad Asif, Mubashir Hassan, Muhammad Faisal, Furhan Iqbal
المصدر: Genes; Volume 13; Issue 11; Pages: 2096
مصطلحات موضوعية: brachyolmia, WES, sanger sequencing, Western blot, 3D protein structure, Genetics, Genetics (clinical)
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c1dce5f09b2e23f050020ce334ef73fTest
https://doi.org/10.3390/genes13112096Test -
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المؤلفون: Simone Pizzi, Daniela Rogaia, Amedea Mencarelli, Giuseppe Merla, Maria Giovanna Tedesco, Valentina Imperatore, Alessandro Bruselles, Elisabetta Flex, Giuseppe Di Cara, Marco Tartaglia, Andrea Ciolfi, Stefania Troiani, Alberto Verrotti, Paolo Prontera, Giovanna Carpentieri
المساهمون: Flex, E., Imperatore, V., Carpentieri, G., Bruselles, A., Ciolfi, A., Pizzi, S., Tedesco, M. G., Rogaia, D., Mencarelli, A., Di Cara, G., Verrotti, A., Troiani, S., Merla, G., Tartaglia, M., Prontera, P.
المصدر: Genes, Vol 12, Iss 1406, p 1406 (2021)
مصطلحات موضوعية: Male, Adolescent, Consanguinity, Biology, QH426-470, whole exome sequencing, Pathogenesis, Genotype-phenotype distinction, consanguinity, Rare Disease, Latent TGF-beta Binding Protein, Peru, medicine, Genetics, Amelogenesis imperfecta, Osteochondrodysplasia, Genetics (clinical), Exome sequencing, Coxa valga, amelogenesis imperfecta, medicine.disease, Pedigree, LTBP3, Hypodontia, stomatognathic diseases, Phenotype, Dysplasia, brachyolmia, medicine.symptom, Human
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1476327de32abd776bcd30df6fe1086Test
https://www.mdpi.com/2073-4425/12/9/1406Test -
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المؤلفون: Madhulika Kabra, Ishrat Siddiqui, Ravneet Kaur, Neerja Gupta, Vijay Prakash Mathur, Manisha Jana
المصدر: American Journal of Medical Genetics Part A. 182:1944-1946
مصطلحات موضوعية: 0301 basic medicine, Genetics, DASS, 030105 genetics & heredity, Biology, medicine.disease, Short stature, Phenotype, Brachyolmia, 03 medical and health sciences, 030104 developmental biology, Dysplasia, medicine, Amelogenesis imperfecta, medicine.symptom, Gene, Genetics (clinical), Function (biology)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0f8f7b776919739b86b55b9e22c17765Test
https://doi.org/10.1002/ajmg.a.61629Test -
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المؤلفون: Satoshi Narumi, Eri Suzuki, Hiroyuki Shinohara, Yukihiro Hasegawa, Masaki Takagi, Mika Shimizu, Gen Nishimura, Tomonobu Hasegawa
المصدر: American Journal of Medical Genetics Part A. 170:795-798
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, DNA Mutational Analysis, Biology, Osteochondrodysplasias, Bone and Bones, 03 medical and health sciences, Genetics, Humans, Exome, Allele, Codon, Collagen Type II, Gene, Alleles, Genetics (clinical), Exome sequencing, Genes, Dominant, Epiphyseal dysplasia, High-Throughput Nucleotide Sequencing, Autosomal dominant brachyolmia, 030104 developmental biology, Amino Acid Substitution, Mutation, Mutation (genetic algorithm)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d00effb72e5b10b549be27b072b3cd7Test
https://doi.org/10.1002/ajmg.a.37481Test -
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المؤلفون: Joe J. Hoo, Michael Oliphant
المصدر: American Journal of Medical Genetics. :80-84
مصطلحات موضوعية: Male, Adolescent, Birth weight, Short stature, Bone and Bones, Brachyolmia, Inheritance Mode, Humans, Medicine, Platyspondyly, Child, Genetics (clinical), Bone Diseases, Developmental, business.industry, Siblings, Puberty, Anatomy, medicine.disease, Osteochondrodysplasia, Short trunk, Short femoral neck, Radiography, Female, medicine.symptom, business, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f469d2c1865c2ea75698898cad5c41fTest
https://doi.org/10.1002/ajmg.a.10875Test -
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المؤلفون: Outi Mäkitie, Nina Jäntti, Stefan Geiberger, Lo Neumeyer, Giedre Grigelioniene, Eva Horemuzova, Eva Bengtsson Moström, Ann Nordgren, Eva Åström, Magnus Nordenskjöld
المصدر: American journal of medical genetics. Part A. (7)
مصطلحات موضوعية: TRPV4, Adult, Male, Pediatrics, medicine.medical_specialty, Genotype, TRPV Cation Channels, Scoliosis, Osteochondrodysplasias, Short stature, Genetics, Medicine, Humans, Platyspondyly, Genetics (clinical), Genetic Association Studies, business.industry, Brachydactyly, Chronic pain, Autosomal dominant brachyolmia, medicine.disease, Phenotype, Spine, Pedigree, Radiography, Child, Preschool, Mutation, Female, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d547fe4a4e1722d7ed7c567b2dc110Test
https://pubmed.ncbi.nlm.nih.gov/24677493Test -
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المؤلفون: Shuji Mizumoto, Gülen Eda Utine, Touma Hoshino, Stefan Geiberger, Pelin Ozlem Simsek-Kiper, Hirofumi Ohashi, Gen Nishimura, Eva Horemuzova, Shigehiko Watanabe, Gozde Yesil, Koray Boduroğlu, Aritoshi Iida, Yasemin Alanay, Nursel Elcioglu, Shiro Ikegawa, Kazuyuki Sugahara, Hülya Kayserili
المساهمون: Acibadem University Dspace, YEŞİL, GÖZDE
المصدر: Human mutation. 34(10)
مصطلحات موضوعية: Male, Heterozygote, Mutation, Missense, Genes, Recessive, Biology, Compound heterozygosity, Osteochondrodysplasias, Short stature, Consanguinity, Multienzyme Complexes, Genetics, medicine, Missense mutation, Humans, Platyspondyly, splice, Genetics (clinical), Homozygote, PAPSS2, Exons, medicine.disease, Phenotype, Introns, Sulfate Adenylyltransferase, Enzyme Activation, Radiography, Dysplasia, Child, Preschool, brachyolmia, Mutation, Mutation testing, Female, androgen excess, medicine.symptom
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::345a01f750db288a28e3a0524a2c0374Test
https://pubmed.ncbi.nlm.nih.gov/23824674Test -
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المؤلفون: Shiro Ikegawa, Andrea Superti-Furga, Ekkehart Lausch, Bernhard Zabel, Gen Nishimura, Ravi Savarirayan, Masahiro Shiba, Sheila Unger, J. Spranger
المصدر: American journal of medical genetics. Part C, Seminars in medical genetics. (3)
مصطلحات موضوعية: TRPV4, Genetics, Mutation, Pathology, medicine.medical_specialty, Bone Diseases, Developmental, Brachydactyly, TRPV Cation Channels, Autosomal dominant brachyolmia, Spinal muscular atrophy, Biology, medicine.disease, medicine.disease_cause, Phenotype, Spondyloepiphyseal dysplasia Maroteaux type, Dysplasia, medicine, Humans, Hereditary motor and sensory neuropathy, Genetics (clinical), Genes, Dominant
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8f6656abd69854e7430fa910f934789Test
https://pubmed.ncbi.nlm.nih.gov/22791502Test -
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المؤلفون: RA Stein
المصدر: Clinical Genetics. 75:118-119
مصطلحات موضوعية: TRPV4, Genetics, Cilium, Cell volume, Autosomal dominant brachyolmia, Biology, Genetics (clinical), Brachyolmia
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dacb75efe2b612df0b031accf3e20b48Test
https://doi.org/10.1111/j.1399-0004.2008.01140_1.xTest -
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المؤلفون: M.J. Rodovalho, R. Antequera, Chong Ae Kim, Débora Romeo Bertola, Isabel Furquim, Luiz Antônio Nunes Oliveira, Rachel Sayuri Honjo, Lilian Maria José Albano
المصدر: American journal of medical genetics. Part A. (3)
مصطلحات موضوعية: Orthodontics, Adult, Male, Adolescent, business.industry, Amelogenesis Imperfecta, Siblings, Dental dysplasia, Consanguinity, medicine.disease, Osteochondrodysplasia, Spine, Brachyolmia, Musculoskeletal Abnormalities, Radiography, Oral and maxillofacial pathology, Genetics, Medicine, Humans, Amelogenesis imperfecta, business, Child, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c5c8552ca5349d38b432d9a4040c452Test
https://pubmed.ncbi.nlm.nih.gov/19213025Test