000 01425 a2200421 4500
005 20250512095052.0
264 0 _c19700324
008 197003s 0 0 eng d
022 _a0028-4793
024 7 _a10.1056/NEJM197003122821105
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNadler, H L
245 0 0 _aRole of amniocentesis in the intrauterine detection of genetic disorders.
_h[electronic resource]
260 _bThe New England journal of medicine
_cMar 1970
300 _a596-9 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAmnion
650 0 4 _aAmniotic Fluid
_xcytology
650 0 4 _aChromosome Aberrations
_xdiagnosis
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes
650 0 4 _aCulture Techniques
650 0 4 _aDiffuse Cerebral Sclerosis of Schilder
_xdiagnosis
650 0 4 _aDown Syndrome
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aFetal Diseases
_xdiagnosis
650 0 4 _aGestational Age
650 0 4 _aGlucosidases
_xmetabolism
650 0 4 _aGlycogen Storage Disease
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aMetabolism, Inborn Errors
_xdiagnosis
650 0 4 _aMethods
650 0 4 _aPregnancy
650 0 4 _aPunctures
700 1 _aGerbie, A B
773 0 _tThe New England journal of medicine
_gvol. 282
_gno. 11
_gp. 596-9
856 4 0 _uhttps://doi.org/10.1056/NEJM197003122821105
_zAvailable from publisher's website
999 _c4249426
_d4249426