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A case of Adams-Oliver syndrome associated with c.3190_3191del and c.4491 + 1G > T mutations in the DOCK6 gene |
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| | Ling Liu, Mengjie Zhou, Jianmei Mao, Yuqi Deng, Yan Cai | | | Meta Gene. 2022; 31: 100988 | | | [Pubmed] [Google Scholar] [DOI] | | 2 |
Adams–Oliver syndrome, intestinal obstruction and heart defects: a case series of aplasia cutis congenita |
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| | Ihsan Baroudi, Ola Alakhras, Thaer Douri, Nedal Alkhani | | | Oxford Medical Case Reports. 2022; 2022(1) | | | [Pubmed] [Google Scholar] [DOI] | | 3 |
APLASIA CUTIS CONGENITA – A CASE SERIES OF VARIED PRESENTATIONS |
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| | Asha S Khade, Shekhar N Pradhan, Umesh Y Bhoi, Sudarshan P Gaurkar, Liza Borah | | | GLOBAL JOURNAL FOR RESEARCH ANALYSIS. 2022; : 13 | | | [Pubmed] [Google Scholar] [DOI] | | 4 |
Síndrome de Adams-Oliver y complicaciones asociadas: reporte de una familia en Colombia y revisión de la literatura |
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| | Olga Lucía Morales, Jerly Maybelline Díaz, Jorge Hernán Montoya | | | Biomédica. 2022; 42(4): 554 | | | [Pubmed] [Google Scholar] [DOI] | | 5 |
Adams–Oliver Syndrome: A Rare Congenital Disorder |
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| | Sumara Rashid, Saleha Azeem, Samiha Riaz | | | Cureus. 2022; | | | [Pubmed] [Google Scholar] [DOI] | | 6 |
Isolated aplasia cutis congenita: A report of two cases |
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| | Yan Wu,Jun Liu,Qiong Luo | | | Clinical Case Reports. 2021; 9(8) | | | [Pubmed] [Google Scholar] [DOI] | |
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