Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

C Kumps, E D'haenens, J Kerkhof… - European Journal of …, 2023 - nature.com
Tatton-Brown-Rahman syndrome (TBRS; OMIM# 615879) is a rare overgrowth and
intellectual disability (ID) syndrome caused by heterozygous loss-of-function variants in the …
被引用次数：4 相关文章
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[PDF][PDF] Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome

C Kumps, E D'haenens, J Kerkhof… - … Journal of Human …, 2023 - backoffice.biblio.ugent.be
Tatton-Brown-Rahman syndrome (TBRS; OMIM# 615879) is a rare overgrowth and
intellectual disability (ID) syndrome caused by heterozygous loss-of-function variants in the …

Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome.

C Kumps, E D'haenens, J Kerkhof… - European Journal of …, 2023 - europepmc.org
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in
two adults with Tatton-Brown-Rahman syndrome. - Abstract - Europe PMC Sign in | Create an …

[引用][C] Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome

C Kumps, E D'haenens, J Kerkhof… - … journal of human …, 2023 - pubmed.ncbi.nlm.nih.gov
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant
in two adults with Tatton-Brown-Rahman syndrome Methylation signatures in clinically …

[引用][C] Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

C Kumps, E D'haenens… - European …, 2023 - researchinformation.amsterdamumc …
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in
two adults with Tatton-Brown–Rahman syndrome — Amsterdam UMC research portal Skip to …
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[PDF][PDF] Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome

C Kumps, E D'haenens, J Kerkhof… - EUROPEAN …, 2023 - biblio.ugent.be
Tatton-Brown-Rahman syndrome (TBRS; OMIM# 615879) is a rare overgrowth and
intellectual disability (ID) syndrome caused by heterozygous loss-of-function variants in the …
[PDF] ugent.be

[PDF][PDF] Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome

C Kumps, E D'haenens, J Kerkhof… - European Journal of …, 2023 - biblio.ugent.be
Tatton-Brown-Rahman syndrome (TBRS; OMIM# 615879) is a rare overgrowth and
intellectual disability (ID) syndrome caused by heterozygous loss-of-function variants in the …