Publication
| Moser AB, Rasmussen M, Naidu S, Watkins PA, McGuinness M, Hajra AK, Chen G, Raymond G, Liu A, Gordon D, et al, Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups. J Pediatr127(1):13-22 1995 |
| PubMed ID: 7541833 |
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| Records Return:
(4)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM16728 | Female | 27 MO | 1989 | proband | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2; RCDP2 | GM |
| GM16774 | Female | 24 YR | 1989 | mother | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2; RCDP2 | GM |
| GM16776 | Female | 18 MO | 1989 | proband | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2; RCDP2 | GM |
| GM16775 | Male | 27 YR | 1989 | father | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2; RCDP2 | GM |
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