| 000 | 01629 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250515001357.0 | ||
| 264 | 0 | _c20080227 | |
| 008 | 200802s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.30966 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aArdalan, Azarnouche | |
| 245 | 0 | 0 |
_aIntrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cOct 2005 |
||
| 300 |
_a288-93 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Breakage |
| 650 | 0 | 4 | _aChromosome Inversion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 20 _xgenetics |
| 650 | 0 | 4 |
_aCryptorchidism _xdiagnosis |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 |
_aEpilepsy _xdiagnosis |
| 650 | 0 | 4 | _aGenetic Markers |
| 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 |
_aMicrocephaly _xdiagnosis |
| 650 | 0 | 4 | _aRecombination, Genetic |
| 700 | 1 | _aPrieur, Marguerite | |
| 700 | 1 | _aChoiset, Agnès | |
| 700 | 1 | _aTurleau, Catherine | |
| 700 | 1 | _aGoutieres, Françoise | |
| 700 | 1 | _aGirard-Orgeolet, Sylvie | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 138A _gno. 3 _gp. 288-93 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.30966 _zAvailable from publisher's website |
| 999 |
_c15791902 _d15791902 |
||