(Q28235637)

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Molecular analysis of congenital scoliosis: a candidate gene approach

scientific article (publication date: April 2005)

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Molecular analysis of congenital scoliosis: a candidate gene approach (English)

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Melissa K Maisenbacher

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1

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Ji-Soo Han

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2

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Megan L O'brien

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3

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Michael R Tracy

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4

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Bülent Erol

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5

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Alyssa A Schaffer

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6

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John P Dormans

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7

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Elaine H Zackai

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8

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Kenro Kusumi

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9

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language of work or name

English

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publication date

April 2005

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published in

Human Genetics

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volume

116

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issue

5

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page(s)

416-9

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cites work

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15717203

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic scoliosis in families of children with congenital scoliosis.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15717203

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

When body segmentation goes wrong.

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15717203

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital scoliosis and vertebral malformations: characterization of segmental defects for genetic analysis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15717203

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15717203

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

(Q28235637)

Molecular analysis of congenital scoliosis: a candidate gene approach

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