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1
المصدر: Journal of Pediatric Orthopaedics. 17:726-733
مصطلحات موضوعية: Pediatrics, Perinatology and Child Health, Orthopedics and Sports Medicine, General Medicine
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2
المؤلفون: Catherine A. Reiser, Noel R. Dasgupta, Richard M. Pauli, V. Kim Horton
المصدر: American Journal of Medical Genetics. 72:347-350
مصطلحات موضوعية: Down syndrome, medicine.medical_specialty, business.industry, Radiography, Aneuploidy, medicine.disease, female genital diseases and pregnancy complications, Intrauterine death, Acetabular angle, medicine, False positive paradox, Radiology, Trisomy, business, reproductive and urinary physiology, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::94f22a54567e2ab60c5ba6f9a5045def
https://doi.org/10.1002/(sici)1096-8628(19971031)72:3<347::aid-ajmg19>3.0.co;2-t -
3
المؤلفون: Peggy Modaff, V. Kim Horton, Richard M. Pauli
المصدر: Prenatal Diagnosis. 16:525-530
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Pregnancy, business.industry, Not Otherwise Specified, Obstetrics and Gynecology, Prenatal diagnosis, medicine.disease, Osteochondrodysplasia, El Niño, medicine, Achondroplasia, Family history, Medical diagnosis, business, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7d16625dae2a60b460b75e81661c1411
https://doi.org/10.1002/(sici)1097-0223(199606)16:6<525::aid-pd909>3.0.co;2-n -
4
المؤلفون: Marcia C. Willing, Shivanand R. Patil, Manjunath Nimmakayalu, Val C. Sheffield, V. Kim Horton, Peter L. Nagy, Oleg A. Shchelochkov, Nathan Noble, Sara Copeland, Thomas H. Wassink
المصدر: American journal of medical genetics. Part A. (11)
مصطلحات موضوعية: Male, Microcephaly, Biology, Bioinformatics, Sodium Channels, SCN3A, Gene cluster, Genetics, medicine, Humans, Abnormalities, Multiple, Copy-number variation, Child, Genetics (clinical), Genetic Association Studies, In Situ Hybridization, Fluorescence, Comparative Genomic Hybridization, Infant, Newborn, Facies, Infant, medicine.disease, Hypotonia, Child, Preschool, Chromosomes, Human, Pair 2, Multigene Family, Female, medicine.symptom, Chromosome Deletion, Haploinsufficiency, Developmental regression, Comparative genomic hybridization