A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH

SL Bhola; AWM Nieuwint; Kyra Stuurman

doi:10.1002/ccr3.1563

A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH

SL Bhola, AWM Nieuwint, Kyra Stuurman

Clinical Genetics

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

1 Citation (Scopus)

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Original language	Undefined/Unknown
Pages (from-to)	1313-1316
Number of pages	4
Journal	Clinical Case Reports
Volume	6
Issue number	7
DOIs	https://doi.org/10.1002/ccr3.1563
Publication status	Published - 2018

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10.1002/ccr3.1563

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http://hdl.handle.net/1765/109203

Cite this

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title = "A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH",

author = "SL Bhola and AWM Nieuwint and Kyra Stuurman",

year = "2018",

doi = "10.1002/ccr3.1563",

language = "Undefined/Unknown",

volume = "6",

pages = "1313--1316",

journal = "Clinical Case Reports",

issn = "2050-0904",

publisher = "John Wiley & Sons Ltd.",

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T1 - A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH

AU - Bhola, SL

AU - Nieuwint, AWM

AU - Stuurman, Kyra

PY - 2018

Y1 - 2018

U2 - 10.1002/ccr3.1563

DO - 10.1002/ccr3.1563

M3 - Article

SN - 2050-0904

VL - 6

SP - 1313

EP - 1316

JO - Clinical Case Reports

JF - Clinical Case Reports

IS - 7

ER -