000 01679 a2200469 4500
005 20250516012844.0
264 0 _c20110315
008 201103s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.33476
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSehested, Line T
245 0 0 _aDeletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cDec 2010
300 _a3115-9 p.
_bdigital
500 _aPublication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAmenorrhea
_xgenetics
650 0 4 _aCells, Cultured
650 0 4 _aChild
650 0 4 _aChild Development Disorders, Pervasive
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Artificial, Bacterial
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aCytogenetic Analysis
_xmethods
650 0 4 _aDNA
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aLanguage Development Disorders
_xgenetics
650 0 4 _aLymphocytes
_xcytology
650 0 4 _aMale
650 0 4 _aSiblings
700 1 _aMøller, Rikke S
700 1 _aBache, Iben
700 1 _aAndersen, Noemi B
700 1 _aUllmann, Reinhard
700 1 _aTommerup, Niels
700 1 _aTümer, Zeynep
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 152A
_gno. 12
_gp. 3115-9
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.33476
_zAvailable from publisher's website
999 _c20379538
_d20379538