000 01209 a2200349 4500
005 20250511160306.0
264 0 _c19760925
008 197609s 0 0 eng d
022 _a0002-922X
024 7 _a10.1001/archpedi.1976.02120090074014
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMing, P M
245 0 0 _aCytogenetic variants in holoprosencephaly. Report of a case and review of the literature.
_h[electronic resource]
260 _bAmerican journal of diseases of children (1960)
_cAug 1976
300 _a864-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAutopsy
650 0 4 _aBrain
_xpathology
650 0 4 _aChromosomes, Human, 13-15
650 0 4 _aFace
_xabnormalities
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aKaryotyping
650 0 4 _aMyocardium
_xpathology
650 0 4 _aTrisomy
700 1 _aGoodner, D M
700 1 _aPark, T S
773 0 _tAmerican journal of diseases of children (1960)
_gvol. 130
_gno. 8
_gp. 864-7
856 4 0 _uhttps://doi.org/10.1001/archpedi.1976.02120090074014
_zAvailable from publisher's website
999 _c949419
_d949419