Publication
Coffee B, Zhang F, Ceman S, Warren ST, Reines D, Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome. Am J Hum Genet71(4):923-32 2002 |
PubMed ID: 12232854 |
|
Records Return:
(1)
|
|
|
|
Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
GM03200 | Male | 34 YR | FRAGILE X MENTAL RETARDATION SYNDROME | GM |
|
|
|