المؤلفون: Burgos, CM, Ebanks, AH, Lof-Granstrom, A, Holden, KI, Johnson, A, Conner, P, Harting, MT

المصدر: Journal of perinatology : official journal of the California Perinatal Association.

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:158347416Test

المؤلفون: Kiasat, A, Ekstrom, LD, Marsk, R, Lof-Granstrom, A, Gustafsson, UO

المصدر: Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 24(8):975-983

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:149189970Test

المؤلفون: Virtanen, VB, Salo, PP, Gao, J, Lof-Granstrom, A, Milani, L, Metspalu, A, Rintala, RJ, Saarenpaa-Heikkila, O, Pauni, T, Wester, T, Nordenskjold, A, Perola, M, Pakarinen, MP

المصدر: European journal of medical genetics. 62(4):229-234

مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Klinisk medicin, Pediatrik

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:140497547Test

المؤلفون: Virtanen, Valtter B., Salo, Perttu P., Gao, Jia, Lof-Granstrom, Anna, Milani, Lill, Metspalu, Andres, Rintala, Risto J., Saarenpaa-Heikkila, Outi, Pauni, Tiina, Wester, Tomas, Nordenskjold, Agneta, Perola, Markus, Pakarinen, Mikko P.

المصدر: WOS ; WOS:000461467500001

مصطلحات موضوعية: Hirschsprung disease, RET, Genetics, GWAS

وصف الملف: 229-234

العلاقة: EUROPEAN JOURNAL OF MEDICAL GENETICS; 62; http://www.julkari.fi/handle/10024/137817Test

الإتاحة: http://www.julkari.fi/handle/10024/137817Test

المؤلفون: Perttu Salo, Tomas Wester, Anna Lof-Granstrom, Lili Milani, Markus Perola, Tiina Paunio, Mikko P. Pakarinen, Risto Rintala, Jia Cao, Agneta Nordenskjöld, Andres Metspalu, Outi Saarenpää-Heikkilä, Valtter B. Virtanen

المساهمون: Children's Hospital, Lastenkirurgian yksikkö, Clinicum, University of Helsinki, Institute for Molecular Medicine Finland, Quantitative Genetics, Research Programs Unit, Diabetes and Obesity Research Program, Department of Psychiatry, HUS Children and Adolescents

المصدر: European Journal of Medical Genetics

مصطلحات موضوعية: EXPRESSION, Male, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Neuregulin-1, Population, Genome-wide association study, Semaphorins, 030105 genetics & heredity, Biology, Polymorphism, Single Nucleotide, Proto-Oncogene Mas, Frameshift mutation, 03 medical and health sciences, Exon, Gene Frequency, NERVOUS-SYSTEM DEVELOPMENT, Genotype, Genetic model, Genetics, GWAS, Humans, Hirschsprung Disease, Allele, Frameshift Mutation, education, Genetics (clinical), Genetic association, education.field_of_study, MUTATIONS, Proto-Oncogene Proteins c-ret, 1184 Genetics, developmental biology, physiology, Exons, General Medicine, GENE, 3. Good health, 030104 developmental biology, Female, 3111 Biomedicine, RET

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3efa231fe1239a8b86527fc5483a8fTest