[HTML] cell.comFull View

[HTML][HTML] Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - The American Journal of …, 2013 - cell.com
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …
被引用次数：82 相关文章

[引用][C] Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - The American Journal …, 2013 - cir.nii.ac.jp
Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant
Isolated Question-Mark Ears | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …

[引用][C] Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

CJ Gordon, F Petit, PM Kroisel… - American Journal of …, 2013 - repositorio.usp.br
ReP USP - Detalhe do registro: Mutations in endothelin 1 cause recessive auriculocondylar
syndrome and dominant isolated question-mark ears Home About USP Schools USP …

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - American Journal of …, 2013 - europepmc.org
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

CT Gordon, F Petit, PM Kroisel… - … journal of human …, 2013 - pubmed.ncbi.nlm.nih.gov
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …

Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - The American Journal of …, 2013 - infona.pl
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …
[HTML] sciencedirect.com

[HTML][HTML] Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - The American Journal of …, 2013 - Elsevier
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …
[HTML] nih.gov

[HTML][HTML] Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - American Journal of …, 2013 - ncbi.nlm.nih.gov
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.

CT Gordon, F Petit, PM Kroisel, L Jakobsen… - American Journal of …, 2013 - europepmc.org
Auriculocondylar syndrome (ACS) is a rare craniofacial disorder with mandibular hypoplasia
and question-mark ears (QMEs) as major features. QMEs, consisting of a specific defect at …