-
1
المؤلفون: Jan M. Wit, Stephany H Donze, Susanne E. Stalman, Wilma Oostdijk, Gerdine A Kamp, Sjoerd D. Joustra, S.G. Kant, Christiaan de Bruin, Monique Losekoot
المساهمون: Pediatrics, Clinical Genetics
المصدر: Hormone Research in Paediatrics, 92(6), 372-381. Karger
Hormone Research in Paediatrics, 92(6), 372-381. KARGERمصطلحات موضوعية: Male, Endocrinology, Diabetes and Metabolism, Haploinsufficiency, Genetic analysis, Short stature, Endocrinology, Short Stature Homeobox Protein, Gene enhancer mutation, Mesomelia, Genetic screening, Medicine, Humans, Madelung deformity, Enhancer, Child, Gene, Growth Disorders, Retrospective Studies, Sequence Deletion, Genetics, Base Sequence, business.industry, Short stature homeobox-containing gene deficiency, Clinical features, medicine.disease, Enhancer Elements, Genetic, Child, Preschool, Pediatrics, Perinatology and Child Health, Homeobox, Female, medicine.symptom, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d35b918af20c4c3cd46bfe1ed2cb61fTest
https://pure.eur.nl/en/publications/42ed0af8-7d2d-451d-8021-b06b5e7d09a6Test -
2
المصدر: Annals of Paediatric Rheumatology. 3:141
مصطلحات موضوعية: medicine.medical_specialty, business.industry, Polyarteritis nodosa, Genetics, Medicine, Arthritis, Juvenile, Animal Science and Zoology, business, medicine.disease, Dermatology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fdadfb0dc7155104a49320b29e1f3887Test
https://doi.org/10.5455/apr.091520140648Test