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1دورية أكاديمية
المؤلفون: M. C. J. Dekker, A. M. Sadiq, R. Mc Larty, R. M. Mbwasi, M. A. A. P. Willemsen, H. R. Waterham, B. C. Hamel
المصدر: Case Reports in Genetics, Vol 2019 (2019)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: A. M. Ali, R. M. Mbwasi, G. Kinabo, E.-J. Kamsteeg, B. C. Hamel, M. C. J. Dekker
المصدر: Case Reports in Genetics, Vol 2017 (2017)
وصف الملف: electronic resource
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3
المؤلفون: H J, Hendriks, H G, Brunner, T A, Haagen, B C, Hamel
المصدر: American Journal of Medical Genetics. 35:443-446
مصطلحات موضوعية: Foot Deformities, Male, Radiography, Mice, Infant, Newborn, Animals, Brain, Humans, Genes, Recessive, Syndrome, Genetics (clinical)
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4
المؤلفون: B C, Hamel
المصدر: Nederlands tijdschrift voor tandheelkunde. 106(2)
مصطلحات موضوعية: Diagnosis, Differential, Male, Pregnancy, Infant, Newborn, Humans, Female, Genetic Counseling, Registries, Referral and Consultation, Congenital Abnormalities
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::a0b8975a4b84e1204dd413b9c929b157
https://pubmed.ncbi.nlm.nih.gov/11930343 -
5
المؤلفون: G J, Van Buggenhout, J M, Trijbels, R, Wevers, J C, Trommelen, B C, Hamel, H G, Brunner, J P, Fryns
المصدر: Genetic counseling (Geneva, Switzerland). 12(1)
مصطلحات موضوعية: Adult, Male, Phenotype, Metabolic Diseases, Intellectual Disability, Humans, Female, Syndrome
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::37ce482acb866166d72e48845326e4ba
https://pubmed.ncbi.nlm.nih.gov/11332972 -
6
المؤلفون: G J, Van Buggenhout, M J, Descheemaeker, P, Thiry, J C, Trommelen, B C, Hamel, J P, Fryns
المصدر: Genetic counseling (Geneva, Switzerland). 11(4)
مصطلحات موضوعية: Male, Intellectual Disability, Humans, Abnormalities, Multiple, Female, Angelman Syndrome, Middle Aged, Nervous System Diseases
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e974e24f57d71b461355cf6d1028eebd
https://pubmed.ncbi.nlm.nih.gov/11140414 -
7
المؤلفون: B C, Hamel, P, Chiurazzi, H A, Lubs
المصدر: American journal of medical genetics. 94(5)
مصطلحات موضوعية: X Chromosome, Genetic Linkage, Intellectual Disability, Humans, Syndrome
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8
المؤلفون: B C, Hamel, F A, Poppelaars
المصدر: Nederlands tijdschrift voor geneeskunde. 144(36)
مصطلحات موضوعية: Male, X Chromosome, Incidence, Intellectual Disability, Mutation, Humans, Female, Genetic Predisposition to Disease, Genetic Testing, Syndrome, Sex Chromosome Aberrations, Netherlands
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::227cebb9710151fc4b91e9b8fd23d990
https://pubmed.ncbi.nlm.nih.gov/10992892 -
9
المؤلفون: J H, Tuerlings, B C, Hamel
المصدر: Nederlands tijdschrift voor geneeskunde. 144(34)
مصطلحات موضوعية: Humans, Genetic Predisposition to Disease, Genetic Testing, Syndrome, Hand Deformities, Congenital, Referral and Consultation, Netherlands
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::5e1467f130792f9305c1a722f5ea2ded
https://pubmed.ncbi.nlm.nih.gov/10972056 -
10
المؤلفون: W Y, Wong, T K, Eskes, A M, Kuijpers-Jagtman, P H, Spauwen, E A, Steegers, C M, Thomas, B C, Hamel, H J, Blom, R P, Steegers-Theunissen
المصدر: Teratology. 60(5)
مصطلحات موضوعية: Adult, Erythrocytes, Cleft Lip, Infant, Pyridoxine, Fasting, Cleft Palate, Vitamin B 12, Folic Acid, Methionine, Pregnancy, Risk Factors, Case-Control Studies, Child, Preschool, Humans, Female, Homocysteine, Maternal-Fetal Exchange