Heteromorphism 18ph+: With or without reproductive consequences?

Annales de Genetique

Volumn 44, Issue 3, 2001, Pages 139-142

  Tabet, A C ^a   Dupont, J M ^b   Lebbar, A ^b   Couturier Turpin, M H ^a   Feldmann, G ^a   Rabineau, D ^b  

^a BICHAT HOSPITAL   (France)

^b Université Paris 5 René Descartes ^*  (France)

Author keywords

18ph+ variant; Genetic counselling; PRINS technique

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 18P; CHROMOSOME VARIANT; FEMALE; GENETIC COUNSELING; GENITAL SYSTEM; HETEROCHROMATIN; HUMAN; MENTAL DEFICIENCY; PRIMED IN SITU LABELING; RECURRENT ABORTION;

EID: 0034762261     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-3995(01)01079-6     Document Type: Article

References (15)

1. Chromosome specific alpha satellites: Two distinct families on human chromosome 18
2. Parental centromere separation sequence and aneuploidy in the offspring
3. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome
4. The 18ph+ chromosome heteromorphism
5. Is 18ph+ a normal chromosomal variant?
6. 18ph+ is a normal chromosomal variant
7. Variation in alphoid DNA size and trisomy 21: A possible cause of nondisjonction
8. Chromosome 18 variant with increased centromeric tandemly repeated DNA in family
9. A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labelling (PRINS)
10. Rapid in situ detection of chromosomes 21 by the PRINS technique
11. Selection of chromosome-specific primers and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomes
12. Prenatal diagnosis of a heterochromatic 18p+ heteromorphism
13. Heteromorphic variant 18 ph+ analysed by sequential CBG and fluorescent in situ hybridization
14. A new chromosome 18 variant in mother and her malformed child
15. Tandemly repeated DNA sequences of the centromere resulting in 18p+