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1.
Expanded phenotype and cancer risk in patients with Beckwith-Wiedemann spectrum caused by CDKN1C variants.
Am J Med Genet A
; : e63777, 2024 Jun 01.
Article
in English
| MEDLINE | ID: mdl-38822599
2.
Familial Beckwith-Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping.
Am J Med Genet A
; 191(2): 348-356, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36322462
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