Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.

Author:

Brandt C A,Hertz J M,Petersen M B,Vogel F,Noer H,Mikkelsen M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. NI 1600 2350 2155 1950 NI 2100 2660

2. The ring chromosome 13 syndrome;Martin, N.J.; Harvey, P.J.; Pearn, J.H.;Hum Genet,1982

3. Le phenotype [Dr] etude de trois cas de chromosomes D en anneau;Lejeune, J.; Lafourcade, J.; Berger, R.;Ann Genet (Paris),1968

4. Partial deletion and trisomies of chromosome 13; mapping of bands associated with particular malformations;Noel, B.; Quack, B.; Rethore, M.O.;Clin Genet,1976

5. Ring chromosome D(13) associated with multiple congenital malformations;Niebuhr, E.; Ottosen, J.;Ann Genet (Paris),1973

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3. Cromosoma 13 en anillo;Boletín Médico del Hospital Infantil de México;2019-06-13

4. Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype;Molecular Syndromology;2019

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