Association of polycystic ovary syndrome with an interstitial deletion of the long arm of chromosome 11 [del(11)(q21q23.1)]

Experimental and Clinical Endocrinology and Diabetes

Volumn 108, Issue 8, 2000, Pages 519-523

  Meyer, M F ^a   Gerresheim, F ^a   Pfeiffer, A ^a   Epplen, J T ^a   Schatz, H ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

Chromosome 11; del(11)(q21q23.1); Polycystic ovary syndrome; Progesterone receptor

Indexed keywords

ANDROGEN; CYTOCHROME P450; FOLLISTATIN; PROGESTERONE RECEPTOR;

ADULT; ANDROGEN BLOOD LEVEL; ARTICLE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME 15; CHROMOSOME 5; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CYTOGENETICS; FEMALE; HIRSUTISM; HUMAN; HUMAN CELL; MENSTRUAL IRREGULARITY; OVARY POLYCYSTIC DISEASE; PRIORITY JOURNAL;

ADULT; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CRANIOFACIAL ABNORMALITIES; FEMALE; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS; LYMPHOCYTES; POLYCYSTIC OVARY SYNDROME; RECEPTORS, PROGESTERONE;

EID: 0033635123     PISSN: 09477349     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-11023     Document Type: Article

References (34)

1. Peters' anomaly associated with deletion of the long arm of chromosome 11
2. Interstitial deletion of the long arm of chromosome 11
3. Trigonocephaly and the 11q-syndrome
4. Ring-11 chromosome: Phenotype-karyotype correlation with deletion 11q
5. Ebstein anomaly associated with rearrangements of chromosomal region 11q
6. Interstitial deletion 11q. Case report and review of the literature
7. The 11q syndrome
8. Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1
9. Familial polycystic ovarian disease
10. Different patterns of follicular development and luteal function
11. Interstitial deletion of 11q
12. Pseudoachondroplasia with de novo deletion [del(11)(q21 q22.2)]
13. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring
14. Williams-Beuren syndrome: Phenotypic variability and deletions of chromosomes 7, 11 and 22 in a series of 52 patients
15. Partial deletion of long arm of chromosome 11: del (11) (q23)
16. Mosaic normal/unbalanced karyotype and recurrent fetal wastage
17. Interstitial deletion of the long arm of chromosome 11
18. Deux nouveaux cas de monosomie 11q partielle avec point de cassure en 11q24
19. Phenotype and genotype in polycystic ovary syndrome
20. Monosomie partielle par deletion du bras long du chromosome 11: del(11)(q23)
21. Genetic map of the human genome: The autosomes and X, Y and mitochondrial chromosomes
22. 11q-syndrome: Review and report of two cases
23. 11q-syndrome with cleft palate
24. Partial deletion of the long arm of chromosome 11: Ten Japanese children
25. The association of a lymphoreticular malignancy with an 11q deletion: A coincidence or a cancer susceptibility?
26. Partial deletion of long arm of chromosome 11 [del(11)(q23)]: Jacobsen syndrome
27. Fragile site long arm chromosome 16
28. Deletion (11) (q14.1q21)
29. Deletion interstitielle du bras long d'un chromosome 11
30. A case report of partial deletion of long arm of chromosome 11; del(11)(q21q23)
31. Monosomie partielle 11q et trigonocephalie. Un nouveau syndrome
32. Thirty-seven candidate genes for polycystic ovary syndrome: Strongest evidence for linkage is with follistatin
33. Interstitial deletion of the long arm of chromosome 11: Report of a case and review of the literature
34. Diagnostic criteria for polycystic ovary syndrome: Towards a rational approach