Skull development in the muscular dystrophic mouse

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Standard

Skull development in the muscular dystrophic mouse. / Vilmann, H; Kirkeby, S; Moss, M L.

I: European Journal of Orthodontics, Bind 11, Nr. 3, 1989, s. 206-13.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Vilmann, H, Kirkeby, S & Moss, ML 1989, 'Skull development in the muscular dystrophic mouse', European Journal of Orthodontics, bind 11, nr. 3, s. 206-13.

APA

Vilmann, H., Kirkeby, S., & Moss, M. L. (1989). Skull development in the muscular dystrophic mouse. European Journal of Orthodontics, 11(3), 206-13.

Vancouver

Vilmann H, Kirkeby S, Moss ML. Skull development in the muscular dystrophic mouse. European Journal of Orthodontics. 1989;11(3):206-13.

Author

Vilmann, H ; Kirkeby, S ; Moss, M L. / Skull development in the muscular dystrophic mouse. I: European Journal of Orthodontics. 1989 ; Bind 11, Nr. 3. s. 206-13.

Bibtex

@article{830e6dc0f29611ddbf70000ea68e967b,
title = "Skull development in the muscular dystrophic mouse",
abstract = "Roentgencephalometric tracings of skulls of 7-week-old normal and muscular dystrophic mice were compared. A marked size reduction of the dystrophic skulls relative to the normal ones was observed. However, the visceral parts of the dystrophic skull were more reduced in size than the neural parts. Marked differences in shape were also noticed. Differences in angular values were primarily found between skull parts, whereas angles between adjacent bones were remarkably similar in the two groups. Only a few exceptions of this condition were observed, as angles between adjacent bones in the posterior part of the cranial vault of the dystrophic animals differed from those of the normal animals. The observed differences between normal and dystrophic mice skulls may chiefly be explained as the results of differences in the action of diseased and normal muscles on bone.",
author = "H Vilmann and S Kirkeby and Moss, {M L}",
note = "Keywords: Animals; Cephalometry; Facial Bones; Female; Mice; Mice, Inbred C57BL; Mice, Inbred Strains; Muscular Dystrophy, Animal; Skull",
year = "1989",
language = "English",
volume = "11",
pages = "206--13",
journal = "European Journal of Orthodontics",
issn = "0141-5387",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Skull development in the muscular dystrophic mouse

AU - Vilmann, H

AU - Kirkeby, S

AU - Moss, M L

N1 - Keywords: Animals; Cephalometry; Facial Bones; Female; Mice; Mice, Inbred C57BL; Mice, Inbred Strains; Muscular Dystrophy, Animal; Skull

PY - 1989

Y1 - 1989

N2 - Roentgencephalometric tracings of skulls of 7-week-old normal and muscular dystrophic mice were compared. A marked size reduction of the dystrophic skulls relative to the normal ones was observed. However, the visceral parts of the dystrophic skull were more reduced in size than the neural parts. Marked differences in shape were also noticed. Differences in angular values were primarily found between skull parts, whereas angles between adjacent bones were remarkably similar in the two groups. Only a few exceptions of this condition were observed, as angles between adjacent bones in the posterior part of the cranial vault of the dystrophic animals differed from those of the normal animals. The observed differences between normal and dystrophic mice skulls may chiefly be explained as the results of differences in the action of diseased and normal muscles on bone.

AB - Roentgencephalometric tracings of skulls of 7-week-old normal and muscular dystrophic mice were compared. A marked size reduction of the dystrophic skulls relative to the normal ones was observed. However, the visceral parts of the dystrophic skull were more reduced in size than the neural parts. Marked differences in shape were also noticed. Differences in angular values were primarily found between skull parts, whereas angles between adjacent bones were remarkably similar in the two groups. Only a few exceptions of this condition were observed, as angles between adjacent bones in the posterior part of the cranial vault of the dystrophic animals differed from those of the normal animals. The observed differences between normal and dystrophic mice skulls may chiefly be explained as the results of differences in the action of diseased and normal muscles on bone.

M3 - Journal article

C2 - 2792212

VL - 11

SP - 206

EP - 213

JO - European Journal of Orthodontics

JF - European Journal of Orthodontics

SN - 0141-5387

IS - 3

ER -

ID: 10141322