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 |