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Breakpoints around the HOXD cluster result in various limb malformations

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Breakpoints around the HOXD cluster result in various limb malformations. / Dlugaszewska, B; Silahtaroglu, A; Menzel, C; Kübart, S; Cohen, Malene; Mundlos, S; Tümer, Z; Kjær, Klaus Wilbrandt; Friedrich, U; Ropers, H-H; Tommerup, N; Neitzel, H; Kalscheuer, V M.

I: Journal of Medical Genetics, Bind 43, Nr. 2, 2006, s. 111-118.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Dlugaszewska, B, Silahtaroglu, A, Menzel, C, Kübart, S, Cohen, M, Mundlos, S, Tümer, Z, Kjær, KW, Friedrich, U, Ropers, H-H, Tommerup, N, Neitzel, H & Kalscheuer, VM 2006, 'Breakpoints around the HOXD cluster result in various limb malformations', Journal of Medical Genetics, bind 43, nr. 2, s. 111-118. https://doi.org/10.1136/jmg.2005.033555

APA

Dlugaszewska, B., Silahtaroglu, A., Menzel, C., Kübart, S., Cohen, M., Mundlos, S., ... Kalscheuer, V. M. (2006). Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics, 43(2), 111-118. https://doi.org/10.1136/jmg.2005.033555

Vancouver

Dlugaszewska B, Silahtaroglu A, Menzel C, Kübart S, Cohen M, Mundlos S o.a. Breakpoints around the HOXD cluster result in various limb malformations. Journal of Medical Genetics. 2006;43(2):111-118. https://doi.org/10.1136/jmg.2005.033555

Author

Dlugaszewska, B ; Silahtaroglu, A ; Menzel, C ; Kübart, S ; Cohen, Malene ; Mundlos, S ; Tümer, Z ; Kjær, Klaus Wilbrandt ; Friedrich, U ; Ropers, H-H ; Tommerup, N ; Neitzel, H ; Kalscheuer, V M. / Breakpoints around the HOXD cluster result in various limb malformations. I: Journal of Medical Genetics. 2006 ; Bind 43, Nr. 2. s. 111-118.

Bibtex

@article{d5d6ec9070eb11dcbee902004c4f4f50,
title = "Breakpoints around the HOXD cluster result in various limb malformations",
abstract = "Characterisation of disease associated balanced chromosome rearrangements is a promising starting point in the search for candidate genes and regulatory elements.",
keywords = "Adolescent, Adult, Chromosome Breakage, Chromosome Mapping, Chromosomes, Human, Pair 2, Computational Biology, Female, Homeodomain Proteins, Humans, In Situ Hybridization, Fluorescence, Infant, Newborn, Karyotyping, Limb Deformities, Congenital, Male, Multigene Family, Mutation, Transcription Factors",
author = "B Dlugaszewska and A Silahtaroglu and C Menzel and S K{\"u}bart and Malene Cohen and S Mundlos and Z T{\"u}mer and Kj{\ae}r, {Klaus Wilbrandt} and U Friedrich and H-H Ropers and N Tommerup and H Neitzel and Kalscheuer, {V M}",
year = "2006",
doi = "10.1136/jmg.2005.033555",
language = "English",
volume = "43",
pages = "111--118",
journal = "Journal of Medical Genetics",
issn = "0022-2593",
publisher = "B M J Group",
number = "2",

}

RIS

TY - JOUR

T1 - Breakpoints around the HOXD cluster result in various limb malformations

AU - Dlugaszewska, B

AU - Silahtaroglu, A

AU - Menzel, C

AU - Kübart, S

AU - Cohen, Malene

AU - Mundlos, S

AU - Tümer, Z

AU - Kjær, Klaus Wilbrandt

AU - Friedrich, U

AU - Ropers, H-H

AU - Tommerup, N

AU - Neitzel, H

AU - Kalscheuer, V M

PY - 2006

Y1 - 2006

N2 - Characterisation of disease associated balanced chromosome rearrangements is a promising starting point in the search for candidate genes and regulatory elements.

AB - Characterisation of disease associated balanced chromosome rearrangements is a promising starting point in the search for candidate genes and regulatory elements.

KW - Adolescent

KW - Adult

KW - Chromosome Breakage

KW - Chromosome Mapping

KW - Chromosomes, Human, Pair 2

KW - Computational Biology

KW - Female

KW - Homeodomain Proteins

KW - Humans

KW - In Situ Hybridization, Fluorescence

KW - Infant, Newborn

KW - Karyotyping

KW - Limb Deformities, Congenital

KW - Male

KW - Multigene Family

KW - Mutation

KW - Transcription Factors

U2 - 10.1136/jmg.2005.033555

DO - 10.1136/jmg.2005.033555

M3 - Journal article

C2 - 15980115

VL - 43

SP - 111

EP - 118

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 2

ER -

ID: 1200152