المؤلفون: T I, Winarni, A, Utari, F E P, Mundhofir, R J, Hagerman, S M H, Faradz

المصدر: Clinical genetics. 84(6)

مصطلحات موضوعية: Male, Adolescent, Abnormal Karyotype, Sequence Analysis, DNA, Fragile X Mental Retardation Protein, Child Development Disorders, Pervasive, Indonesia, Child, Preschool, Fragile X Syndrome, Cytogenetic Analysis, Mutation, Prevalence, Humans, Female, Genetic Testing, Child

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0d8c652cf0dd6b09f085011e048db1f8
https://pubmed.ncbi.nlm.nih.gov/23320543

المؤلفون: T I, Winarni, F E P, Mundhofir, A, Ediati, M, Belladona, W M, Nillesen, H G, Yntema, B C J, Hamel, S M H, Faradz, R J, Hagerman

المصدر: Clinical genetics. 83(3)

مصطلحات موضوعية: Family Health, Male, Syndrome, Middle Aged, Neuropsychological Tests, Pedigree, Fragile X Mental Retardation Protein, Indonesia, Fragile X Syndrome, Tremor, Humans, Ataxia, Female, Genetic Predisposition to Disease, Trinucleotide Repeat Expansion, Aged

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::33d9d1aa7be72b5e0e03648510047d99
https://pubmed.ncbi.nlm.nih.gov/22568721

المؤلفون: F E P, Mundhofir, A J A, Kooper, T I, Winarni, A P T, Smits, S M H, Faradz, B C J, Hamel

المصدر: Genetic counseling (Geneva, Switzerland). 21(1)

مصطلحات موضوعية: Family Health, Male, Chromosomes, Human, Pair 22, Intellectual Disability, Skull, Humans, Abnormalities, Multiple, Trisomy, Child, Facial Bones, Translocation, Genetic, Chromosomes, Human, Pair 8, Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::698293b1068bdd89af82362dc3a1d0d2
https://pubmed.ncbi.nlm.nih.gov/20420036