Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.

M J Macera; A Sobrino; B Levy; V Jobanputra; V Aggarwal; A Mills; C Esteves; C Hanscom; S Pereira; V Pillalamarri; Z Ordulu; C C Morton; M Talkowski; D Warburton

doi:10.1002/pd.4456

Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.

M J Macera, A Sobrino, B Levy, V Jobanputra, V Aggarwal, A Mills, C Esteves, C Hanscom, S Pereira, V Pillalamarri, Z Ordulu, C C Morton, M Talkowski, D Warburton

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

Original language	English
Journal	Prenatal diagnosis
Volume	35
Issue number	3
DOIs	https://doi.org/10.1002/pd.4456
Publication status	Published - Mar 2015

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10.1002/pd.4456

Manchester Centre for Audiology and Deafness (ManCAD)
Munro, K. (PI), Millman, R. (PI), Lamb, W. (Support team), Dawes, P. (PI), Plack, C. (PI), Stone, M. (PI), Kluk-De Kort, K. (PI), Moore, D. (PI), Morton, C. (PI), Prendergast, G. (PI), Couth, S. (PI), Schlittenlacher, J. (PI), Chilton, H. (PI), Visram, A. (Researcher), Dillon, H. (PI), Guest, H. (Researcher), Heinrich, A. (PI), Jackson, I. (Researcher), Littlejohn, J. (Researcher), Jones, L. (PI), Lough, M. (Researcher), Morgan, R. (Researcher), Perugia, E. (Researcher), Roughley, A. (Researcher), Whiston, H. (Researcher), Wright, C. (Support team), Saunders, G. (PI), Kelly, C. (PI), Cross, H. (Researcher), Loughran, M. (Researcher), Hoseinabadi, R. (PI) & Vercammen, C. (PI)
Project: Research

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Macera, M. J., Sobrino, A., Levy, B., Jobanputra, V., Aggarwal, V., Mills, A., Esteves, C., Hanscom, C., Pereira, S., Pillalamarri, V., Ordulu, Z., Morton, C. C., Talkowski, M., & Warburton, D. (2015). Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing. Prenatal diagnosis, 35(3). https://doi.org/10.1002/pd.4456

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title = "Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.",

author = "Macera, {M J} and A Sobrino and B Levy and V Jobanputra and V Aggarwal and A Mills and C Esteves and C Hanscom and S Pereira and V Pillalamarri and Z Ordulu and Morton, {C C} and M Talkowski and D Warburton",

note = "K99 MH095867, NIMH NIH HHS, United StatesP01 GM061354, NIGMS NIH HHS, United StatesP01GM061354, NIGMS NIH HHS, United StatesR00MH095867, NIMH NIH HHS, United States",

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doi = "10.1002/pd.4456",

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Macera, MJ, Sobrino, A, Levy, B, Jobanputra, V, Aggarwal, V, Mills, A, Esteves, C, Hanscom, C, Pereira, S, Pillalamarri, V, Ordulu, Z, Morton, CC, Talkowski, M & Warburton, D 2015, 'Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.', Prenatal diagnosis, vol. 35, no. 3. https://doi.org/10.1002/pd.4456

TY - JOUR

T1 - Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.

AU - Macera, M J

AU - Sobrino, A

AU - Levy, B

AU - Jobanputra, V

AU - Aggarwal, V

AU - Mills, A

AU - Esteves, C

AU - Hanscom, C

AU - Pereira, S

AU - Pillalamarri, V

AU - Ordulu, Z

AU - Morton, C C

AU - Talkowski, M

AU - Warburton, D

N1 - K99 MH095867, NIMH NIH HHS, United StatesP01 GM061354, NIGMS NIH HHS, United StatesP01GM061354, NIGMS NIH HHS, United StatesR00MH095867, NIMH NIH HHS, United States

PY - 2015/3

Y1 - 2015/3

U2 - 10.1002/pd.4456

DO - 10.1002/pd.4456

M3 - Article

C2 - 25043231

SN - 1097-0223

VL - 35

JO - Prenatal diagnosis

JF - Prenatal diagnosis

IS - 3

ER -

Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.

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Manchester Centre for Audiology and Deafness (ManCAD)

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