A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.

Bente Talseth-Palmer; Nikola Bowden; Cliff Meldrum; Jillian Nicholl; Elizabeth Thompson; K Friend; J Liebelt; Drago Bratkovic; Eric Haan; S Yu; Rodney Scott

A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.

Bente Talseth-Palmer
, Nikola Bowden
, Cliff Meldrum
, Jillian Nicholl
, Elizabeth Thompson
, K Friend
, J Liebelt
, Drago Bratkovic
, Eric Haan
, S Yu
, Rodney Scott

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

6 Citations (Scopus)

Original language	English
Pages (from-to)	94-101
Number of pages	8
Journal	CYTOGENETIC AND GENOME RESEARCH
Volume	124
Issue number	1
Publication status	Published - 2009

Cite this

@article{ee0f5bf755fa4ca596c8669609ce0f63,

title = "A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.",

author = "Bente Talseth-Palmer and Nikola Bowden and Cliff Meldrum and Jillian Nicholl and Elizabeth Thompson and K Friend and J Liebelt and Drago Bratkovic and Eric Haan and S Yu and Rodney Scott",

year = "2009",

language = "English",

volume = "124",

pages = "94--101",

journal = "CYTOGENETIC AND GENOME RESEARCH",

issn = "1424-8581",

publisher = "S. Karger AG",

number = "1",

}

Talseth-Palmer, B, Bowden, N, Meldrum, C, Nicholl, J, Thompson, E, Friend, K, Liebelt, J, Bratkovic, D, Haan, E, Yu, S & Scott, R 2009, 'A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.', CYTOGENETIC AND GENOME RESEARCH, vol. 124, no. 1, pp. 94-101.

A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology. / Talseth-Palmer, Bente; Bowden, Nikola; Meldrum, Cliff et al.
In: CYTOGENETIC AND GENOME RESEARCH, Vol. 124, No. 1, 2009, p. 94-101.

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

TY - JOUR

T1 - A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.

AU - Talseth-Palmer, Bente

AU - Bowden, Nikola

AU - Meldrum, Cliff

AU - Nicholl, Jillian

AU - Thompson, Elizabeth

AU - Friend, K

AU - Liebelt, J

AU - Bratkovic, Drago

AU - Haan, Eric

AU - Yu, S

AU - Scott, Rodney

PY - 2009

Y1 - 2009

M3 - Article

SN - 1424-8581

VL - 124

SP - 94

EP - 101

JO - CYTOGENETIC AND GENOME RESEARCH

JF - CYTOGENETIC AND GENOME RESEARCH

IS - 1

ER -