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8q22-q23
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
OBJECTIVE
We present prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins… Expand
2017
2017
El sindrome de Cohen (SC) es una enfermedad genetica rara, con herencia autosomica recesiva. Se origina por danos en el gen… Expand
2006
2006
Objective: To investigate underlying genetic events associated with complex DNA ploidy breast carcinomas. Methods: Screening for… Expand
2004
2004
We describe eight members from two large Amish kindreds who share a phenotype characterized by early‐onset pigmentary retinopathy… Expand
Highly Cited
2003
Highly Cited
2003
Conventional cytogenetic and comparative genomic hybridization (CGH) studies have shown that osteosarcomas (OSs) are… Expand
2002
2002
Superficial lipomas are very common benign adipose tissue tumors. In contrast, deep-seated lipomas such as retroperitoneal… Expand
2001
2001
We have developed an integrated map for a 35-cM area of human chromosome 8 surrounding the Langer-Giedion syndrome deletion… Expand
2000
2000
Endometrial cancer progression is determined by a complex pattern of multiple genetic aberrations, but how these aberrations… Expand
1997
1997
The INT6 gene is a common integration site for the mouse mammary tumor virus in mouse mammary tumors. We have determined that the… Expand