Family NIGMS00058 Members
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Records Return:
(4)
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Catalog ID | Description | Sex | Age | Race | Affected | Family Member | Relationship to Proband | Cell Type | Family |
GM29125 | CHROMOSOME XP11.3 DELETION SYNDROME | Male | 34 YR | White | No | 2 | father | B-Lymphocyte | NIGMS00058 |
GM29126 | CHROMOSOME XP11.3 DELETION SYNDROME | Male | 3 YR | White | Yes | 1 | proband | B-Lymphocyte | NIGMS00058 |
GM29277 | CHROMOSOME XP11.3 DELETION SYNDROME | Male | 3 YR | White | Yes | 1 | proband | Stem cell | NIGMS00058 |
GM29310 | CHROMOSOME XP11.3 DELETION SYNDROME | Male | 34 YR | White | No | 2 | father | Stem cell | NIGMS00058 |
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