Publication
| Hall CR, Wu Y, Shaffer LG, Hecht JT, Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4 Clinical genetics60:356-9 2002 |
| PubMed ID: 11903336 |
|
| Records Return:
(1)
|
|
|
|
|
| Catalog ID | Gender | Description | Collection_Type_id |
| GM22627 | Male | POTOCKI-SHAFFER SYNDROME | GM |
|
|
|