A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

Marja Wessels; Bianca de Graaf; Titia Overbeek; SEC (Silja) Spitaels; Lotte Laat; Folkert ten Cate; Ingrid Mulder; Ronald de Krijger; MM Bartelings; N Essed; Juriy Wladimiroff; Martinus Niermeijer; P Heutink; Ben Oostra; D Dooijes; AM Bertoli Avella; PJ Willems

doi:10.1007/s00439-007-0436-x

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

Marja Wessels, Bianca de Graaf, Titia Overbeek, SEC (Silja) Spitaels, Lotte Laat, Folkert ten Cate, Ingrid Mulder, Ronald de Krijger, MM Bartelings, N Essed, Juriy Wladimiroff, Martinus Niermeijer, P Heutink, Ben Oostra, D Dooijes, AM Bertoli Avella, PJ Willems

Research output: Contribution to journal › Article › Academic › peer-review

33 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	595-603
Number of pages	9
Journal	Human Genetics
Volume	122
DOIs	https://doi.org/10.1007/s00439-007-0436-x
Publication status	Published - 2008

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10.1007/s00439-007-0436-x

http://hdl.handle.net/1765/29624

Cite this

Wessels, M., de Graaf, B., Overbeek, T., Spitaels, SEC., Laat, L., ten Cate, F., Mulder, I., de Krijger, R., Bartelings, MM., Essed, N., Wladimiroff, J., Niermeijer, M., Heutink, P., Oostra, B., Dooijes, D., Bertoli Avella, AM., & Willems, PJ. (2008). A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p. Human Genetics, 122, 595-603. https://doi.org/10.1007/s00439-007-0436-x

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title = "A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p",

author = "Marja Wessels and {de Graaf}, Bianca and Titia Overbeek and Spitaels, {SEC (Silja)} and Lotte Laat and {ten Cate}, Folkert and Ingrid Mulder and {de Krijger}, Ronald and MM Bartelings and N Essed and Juriy Wladimiroff and Martinus Niermeijer and P Heutink and Ben Oostra and D Dooijes and {Bertoli Avella}, AM and PJ Willems",

year = "2008",

doi = "10.1007/s00439-007-0436-x",

language = "Undefined/Unknown",

volume = "122",

pages = "595--603",

journal = "Human Genetics",

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Wessels, M, de Graaf, B, Overbeek, T, Spitaels, SEC, Laat, L, ten Cate, F, Mulder, I, de Krijger, R, Bartelings, MM, Essed, N, Wladimiroff, J, Niermeijer, M, Heutink, P, Oostra, B, Dooijes, D, Bertoli Avella, AM & Willems, PJ 2008, 'A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p', Human Genetics, vol. 122, pp. 595-603. https://doi.org/10.1007/s00439-007-0436-x

TY - JOUR

T1 - A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

AU - Wessels, Marja

AU - de Graaf, Bianca

AU - Overbeek, Titia

AU - Spitaels, SEC (Silja)

AU - Laat, Lotte

AU - ten Cate, Folkert

AU - Mulder, Ingrid

AU - de Krijger, Ronald

AU - Bartelings, MM

AU - Essed, N

AU - Wladimiroff, Juriy

AU - Niermeijer, Martinus

AU - Heutink, P

AU - Oostra, Ben

AU - Dooijes, D

AU - Bertoli Avella, AM

AU - Willems, PJ

PY - 2008

Y1 - 2008

U2 - 10.1007/s00439-007-0436-x

DO - 10.1007/s00439-007-0436-x

M3 - Article

SN - 0340-6717

VL - 122

SP - 595

EP - 603

JO - Human Genetics

JF - Human Genetics

ER -