deletion mosaic associated literature 13q phenotype rb1 mild outcome cancer including case report review
deletion tumors chromosome 13q rb1
balanced moroccan hereditary 13q retinoblastoma deletion intellectual interstitial disability assumption insertion fragment
syndrome 13q significance parental balanced chromosomal rearrangement resulting karyotyping framework implementation citation
figure 13q deletion cases medical journal root thin dysmorphic prominent downturned triangular lip nasal forehead include upper features face high
rb1 loss pituitary protein infrequent 13q despite deletion mapping retinoblastoma susceptibility tumors chromosome gene locus
deletion 13q chronic lymphocytic leukemia progression