000 | 01135 a2200373 4500 | ||
---|---|---|---|
005 | 20250512084516.0 | ||
264 | 0 | _c19851029 | |
008 | 198510s 0 0 eng d | ||
022 | _a0547-6844 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aJaramillo, C | |
245 | 0 | 0 |
_aChromosomal diagnosis of the Werner syndrome. _h[electronic resource] |
260 |
_bBirth defects original article series _c1985 |
||
300 |
_a119-26 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChromosomes, Human, 16-18 |
650 | 0 | 4 | _aChromosomes, Human, 19-20 |
650 | 0 | 4 | _aDiagnosis, Differential |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 | _aMosaicism |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 |
_aScleroderma, Systemic _xdiagnosis |
650 | 0 | 4 | _aTranslocation, Genetic |
650 | 0 | 4 |
_aTurner Syndrome _xdiagnosis |
650 | 0 | 4 |
_aWerner Syndrome _xdiagnosis |
650 | 0 | 4 | _aX Chromosome |
700 | 1 | _aJorgenson, R J | |
700 | 1 | _aMiles, D A | |
700 | 1 | _aMoore, C M | |
773 | 0 |
_tBirth defects original article series _gvol. 21 _gno. 2 _gp. 119-26 |
|
999 |
_c4047256 _d4047256 |