Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.

Bisgaard Am, Kirchhoff M, Nielsen Je, Kibaek M, Lund A, Schwartz M, Christensen E

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Adgang til dokumentet

@article{a64a9af35a604a2ea98f2a425d1b667a,

title = "Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.",

author = "Bisgaard Am and Kirchhoff M and Nielsen Je and Kibaek M and Lund A and Schwartz M and Christensen E",

year = "2009",

month = feb,

day = "1",

doi = "10.1111/j.1399-0004.2008.01113.x",

language = "Udefineret/Ukendt",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell",

}

TY - JOUR

T1 - Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.

AU - Am, Bisgaard

AU - M, Kirchhoff

AU - Je, Nielsen

AU - M, Kibaek

AU - A, Lund

AU - M, Schwartz

AU - E, Christensen

PY - 2009/2/1

Y1 - 2009/2/1

U2 - 10.1111/j.1399-0004.2008.01113.x

DO - 10.1111/j.1399-0004.2008.01113.x

M3 - Tidsskriftartikel

SN - 0009-9163

JO - Clinical Genetics

JF - Clinical Genetics

ER -