[HTML] spandidos-publications.com

[HTML][HTML] First documented case of Myhre syndrome in Romania: A case report

A Cătană, R Simonescu‑Colan… - Experimental and …, 2022 - spandidos-publications.com
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …
被引用次数：3 相关文章
[PDF] academia.edu

[PDF][PDF] First documented case of Myhre syndrome in Romania: A case report

A CĂTANĂ, R SIMONESCU‑COLAN… - EXPERIMENTAL AND …, 2022 - academia.edu
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by devel‑opmental delay, characteristic facial features, various bone and joint …
[HTML] nih.gov

[HTML][HTML] First documented case of Myhre syndrome in Romania: A case report

A Cătană, R Simonescu-Colan… - Experimental and …, 2022 - ncbi.nlm.nih.gov
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …

First documented case of Myhre syndrome in Romania: A case report

A Cătană, R Simonescu-Colan… - Experimental and …, 2022 - pubmed.ncbi.nlm.nih.gov
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …

First documented case of Myhre syndrome in Romania: A case report.

A Cătană, R Simonescu-Colan… - Experimental & …, 2022 - search.ebscohost.com
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …

First documented case of Myhre syndrome in Romania: A case report.

A Cătană, R Simonescu-Colan… - Experimental and …, 2022 - europepmc.org
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …

First documented case of Myhre syndrome in Romania: A case report

A CĂTANĂ, R SIMONESCU‑COLAN… - EXPERIMENTAL …, 2022 - ingentaconnect.com
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …

First documented case of Myhre syndrome in Romania: A case report.

A Cătană, R Simonescu-Colan… - Experimental and …, 2022 - europepmc.org
Myhre syndrome is a rare genetic autosomal dominant connective tissue disorder,
characterized by developmental delay, characteristic facial features, various bone and joint …