| 000 | 01723 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250513160036.0 | ||
| 264 | 0 | _c19990217 | |
| 008 | 199902s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/(sici)1096-8628(19981204)80:4<377::aid-ajmg14>3.0.co;2-7 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGoodman, B K | |
| 245 | 0 | 0 |
_aInherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cDec 1998 |
||
| 300 |
_a377-84 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGrowth Disorders _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMuscle Hypotonia _xgenetics |
| 650 | 0 | 4 |
_aX Chromosome _xgenetics |
| 700 | 1 | _aShaffer, L G | |
| 700 | 1 | _aRutberg, J | |
| 700 | 1 | _aLeppert, M | |
| 700 | 1 | _aHarum, K | |
| 700 | 1 | _aGagos, S | |
| 700 | 1 | _aRay, J H | |
| 700 | 1 | _aBialer, M G | |
| 700 | 1 | _aZhou, X | |
| 700 | 1 | _aPletcher, B A | |
| 700 | 1 | _aShapira, S K | |
| 700 | 1 | _aGeraghty, M T | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 80 _gno. 4 _gp. 377-84 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(sici)1096-8628(19981204)80:4<377::aid-ajmg14>3.0.co;2-7 _zAvailable from publisher's website |
| 999 |
_c9819649 _d9819649 |
||