000 01903 a2200529 4500
005 20250516041034.0
264 0 _c20111018
008 201110s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/1750-1172-6-32
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRall, Katharina
245 0 0 _aA combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cMay 2011
300 _a32 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _a46, XX Disorders of Sex Development
_xembryology
650 0 4 _aAbnormalities, Multiple
_xembryology
650 0 4 _aCongenital Abnormalities
650 0 4 _aCpG Islands
_xgenetics
650 0 4 _aDNA Methylation
650 0 4 _aFemale
650 0 4 _aGene Expression Profiling
650 0 4 _aGene Expression Regulation, Developmental
_xphysiology
650 0 4 _aHumans
650 0 4 _aKidney
_xabnormalities
650 0 4 _aMullerian Ducts
_xabnormalities
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aReproducibility of Results
650 0 4 _aReverse Transcriptase Polymerase Chain Reaction
650 0 4 _aSomites
_xabnormalities
650 0 4 _aSpine
_xabnormalities
650 0 4 _aUterus
_xabnormalities
650 0 4 _aVagina
_xabnormalities
700 1 _aBarresi, Gianmaria
700 1 _aWalter, Michael
700 1 _aPoths, Sven
700 1 _aHaebig, Karina
700 1 _aSchaeferhoff, Karin
700 1 _aSchoenfisch, Birgitt
700 1 _aRiess, Olaf
700 1 _aWallwiener, Diethelm
700 1 _aBonin, Michael
700 1 _aBrucker, Sara
773 0 _tOrphanet journal of rare diseases
_gvol. 6
_gp. 32
856 4 0 _uhttps://doi.org/10.1186/1750-1172-6-32
_zAvailable from publisher's website
999 _c20880090
_d20880090