000 01150 a2200385 4500
005 20250511154622.0
264 0 _c19770929
008 197709s 0 0 fre d
022 _a0031-4021
040 _aNLM
_beng
_cNLM
100 1 _aLarget-Piet, L
245 0 0 _a[Prenatal detection of genetic diseases. Experience with 317 diagnoses].
_h[electronic resource]
260 _bPediatrie
_cJun 1977
300 _a313-22 p.
_bdigital
500 _aPublication Type: English Abstract; Journal Article
650 0 4 _aAmniocentesis
650 0 4 _aChromosome Aberrations
_xdiagnosis
650 0 4 _aChromosome Disorders
650 0 4 _aCongenital Abnormalities
_xdiagnosis
650 0 4 _aCytogenetics
650 0 4 _aFemale
650 0 4 _aGenetic Diseases, Inborn
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aMetabolism, Inborn Errors
_xdiagnosis
650 0 4 _aPregnancy
700 1 _aBerthelot, J
700 1 _aDenis, A
700 1 _aDaver, A
700 1 _aLarget-Piet, A
700 1 _aBeucher, A
700 1 _aLe Marec, B
700 1 _aLe Lirzin, R
700 1 _aRouchy, R
773 0 _tPediatrie
_gvol. 32
_gno. 4
_gp. 313-22
999 _c894919
_d894919