Ring chromosome 13 in an infant with ambiguous genitalia.
Sankar, V H; Phadke, Shubha R.
Indian Pediatr
; 2006 Mar; 43(3): 258-60
Artículo en Inglés | IMSEAR | ID: sea-13678
Documentos relacionados
Ring chromosome 13 in an infant with ambiguous genitalia.
Disorder of sex development in a cat with chromosome mosaicism 37,X/38,X,r(Y).
Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review.
Mosaic r(13) in an infant with aprosencephaly.
Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism.
Ring chromosome 13 and ambiguous genitalia.
Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature.
Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
[Clinical and genetic features of ring chromosome 13 syndrome: an analysis of one case].