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