A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

R van de Putte; GC Dworschak; Erwin Brosens; HM Reutter; CL Marcelis; R Acuna-Hidalgo; NE Kurtas; M Steehouwer; SL Dunwoodie; E Schmiedeke; S Marzheuser; N Schwarzer; Alice Brooks; Annelies de Klein; C.E.J. Sloots; Dick Tibboel; G Brisighelli; A Morandi; MF Bedeschi; MD Bates; MA Levitt; A de la Pena; I de Blaauw; N Roeleveld; HG Brunner; I de Rooij; A Hoischen

doi:10.3389/fped.2020.00310

A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

R van de Putte, GC Dworschak, Erwin Brosens, HM Reutter, CL Marcelis, R Acuna-Hidalgo, NE Kurtas, M Steehouwer, SL Dunwoodie, E Schmiedeke, S Marzheuser, N Schwarzer, Alice Brooks, Annelies de Klein, C.E.J. Sloots, Dick Tibboel, G Brisighelli, A Morandi, MF Bedeschi, MD BatesMA Levitt, A de la Pena, I de Blaauw, N Roeleveld, HG Brunner, I de Rooij, A Hoischen

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

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Original language	English
Article number	310
Journal	Frontiers in Pediatrics
Volume	8
DOIs	https://doi.org/10.3389/fped.2020.00310
Publication status	Published - 2020

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EMC OR-01

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10.3389/fped.2020.00310

Repub_128749_O-A.pdfFinal published version, 233 KB

http://hdl.handle.net/1765/128749

Cite this

van de Putte, R., Dworschak, GC., Brosens, E., Reutter, HM., Marcelis, CL., Acuna-Hidalgo, R., Kurtas, NE., Steehouwer, M., Dunwoodie, SL., Schmiedeke, E., Marzheuser, S., Schwarzer, N., Brooks, A., de Klein, A., Sloots, C. E. J., Tibboel, D., Brisighelli, G., Morandi, A., Bedeschi, MF., ... Hoischen, A. (2020). A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in Pediatrics, 8, Article 310. https://doi.org/10.3389/fped.2020.00310

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title = "A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies",

author = "{van de Putte}, R and GC Dworschak and Erwin Brosens and HM Reutter and CL Marcelis and R Acuna-Hidalgo and NE Kurtas and M Steehouwer and SL Dunwoodie and E Schmiedeke and S Marzheuser and N Schwarzer and Alice Brooks and {de Klein}, Annelies and C.E.J. Sloots and Dick Tibboel and G Brisighelli and A Morandi and MF Bedeschi and MD Bates and MA Levitt and {de la Pena}, A and {de Blaauw}, I and N Roeleveld and HG Brunner and {de Rooij}, I and A Hoischen",

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van de Putte, R, Dworschak, GC, Brosens, E, Reutter, HM, Marcelis, CL, Acuna-Hidalgo, R, Kurtas, NE, Steehouwer, M, Dunwoodie, SL, Schmiedeke, E, Marzheuser, S, Schwarzer, N, Brooks, A , de Klein, A , Sloots, CEJ , Tibboel, D, Brisighelli, G, Morandi, A, Bedeschi, MF, Bates, MD, Levitt, MA, de la Pena, A, de Blaauw, I, Roeleveld, N, Brunner, HG, de Rooij, I & Hoischen, A 2020, 'A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies', Frontiers in Pediatrics, vol. 8, 310. https://doi.org/10.3389/fped.2020.00310

TY - JOUR

T1 - A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

AU - van de Putte, R

AU - Dworschak, GC

AU - Brosens, Erwin

AU - Reutter, HM

AU - Marcelis, CL

AU - Acuna-Hidalgo, R

AU - Kurtas, NE

AU - Steehouwer, M

AU - Dunwoodie, SL

AU - Schmiedeke, E

AU - Marzheuser, S

AU - Schwarzer, N

AU - Brooks, Alice

AU - de Klein, Annelies

AU - Sloots, C.E.J.

AU - Tibboel, Dick

AU - Brisighelli, G

AU - Morandi, A

AU - Bedeschi, MF

AU - Bates, MD

AU - Levitt, MA

AU - de la Pena, A

AU - de Blaauw, I

AU - Roeleveld, N

AU - Brunner, HG

AU - de Rooij, I

AU - Hoischen, A

PY - 2020

Y1 - 2020

U2 - 10.3389/fped.2020.00310

DO - 10.3389/fped.2020.00310

M3 - Article

C2 - 32656166

SN - 2296-2360

VL - 8

JO - Frontiers in Pediatrics

JF - Frontiers in Pediatrics

M1 - 310

ER -