Mental retardation with rare fragile site expressed at 2q11

Brain and Development

Volumn 22, Issue 8, 2000, Pages 498-500

  Tükün, Ajlan ^a   Renda, Yavuz ^b   Topçu, Meral ^b   Tuncali, Timur ^a   Bökesoy, Isik ^a  

^a ANKARA UNIVERSITY   (Turkey)

^b HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Autosomes; Chromosome 2; Fra (2)(q11); Mental retardation; Rare folate sensitive fragile sites

Indexed keywords

ARTICLE; AUTOSOME; CASE REPORT; CHILD; CHROMOSOME 2; CHROMOSOME ANALYSIS; CHROMOSOME FRAGILE SITE; CONGENITAL MALFORMATION; FEMALE; FRAGILE X SYNDROME; HUMAN; MENTAL DEFICIENCY; PHENOTYPE;

CHILD; CHROMOSOME FRAGILE SITES; CHROMOSOME FRAGILITY; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; HUMANS; MENTAL RETARDATION; PHENOTYPE;

EID: 0033678866     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(00)00189-3     Document Type: Article

References (10)

1. The detection of fragile sites on human chromosomes
2. Fragile sites still breaking
3. Population cytogenetics of autosomal fragile sites
4. Possible association of rare autosomal folate sensitive fragile sites and idiopathic mental retardation: a blind controlled population study
5. Are some multiple congenital anomalies with mental retardation (MCA/MR) the clinical expression of rare autosomal fragile sites?
6. Frequency of rare fragile sites among mentally subnormal schoolchildren
7. Letters to the Editor: Population cytogenetics of autosomal fragile sites
8. Chromosomal fragile site expression in lymphocytes from patients with schizophrenia
9. Human Genetics'99: Trinucleotide repeats. Fragile sites-cytogenetic similarity with molecular diversity
10. Long CCG repeat blocks exclude nucleosomes: a possible mechanism for the nature of fragile sites in chromosomes