000 01162 a2200349 4500
005 20250513235241.0
264 0 _c20010823
008 200108s 0 0 eng d
022 _a0962-8827
024 7 _a10.1097/00019605-200104000-00012
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLammer, E J
245 0 0 _aInherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome.
_h[electronic resource]
260 _bClinical dysmorphology
_cApr 2001
300 _a141-4 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aGenes, Duplicate
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aPrader-Willi Syndrome
_xgenetics
650 0 4 _aSex Chromosome Aberrations
_xgenetics
650 0 4 _aX Chromosome
700 1 _aPunglia, D R
700 1 _aFuchs, A E
700 1 _aRowe, A G
700 1 _aCotter, P D
773 0 _tClinical dysmorphology
_gvol. 10
_gno. 2
_gp. 141-4
856 4 0 _uhttps://doi.org/10.1097/00019605-200104000-00012
_zAvailable from publisher's website
999 _c11245606
_d11245606