000 | 01103 a2200325 4500 | ||
---|---|---|---|
005 | 20250513005356.0 | ||
264 | 0 | _c19820621 | |
008 | 198206s 0 0 eng d | ||
022 | _a0022-2593 | ||
024 | 7 |
_a10.1136/jmg.19.1.78 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aGaba, A R | |
245 | 0 | 0 |
_aAlobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis. _h[electronic resource] |
260 |
_bJournal of medical genetics _cFeb 1982 |
||
300 |
_a78 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human _xultrastructure |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 |
_aPlacenta Diseases _xgenetics |
650 | 0 | 4 | _aPregnancy |
700 | 1 | _aAnderson, G J | |
700 | 1 | _aVanDyke, D L | |
700 | 1 | _aChason, J L | |
773 | 0 |
_tJournal of medical genetics _gvol. 19 _gno. 1 _gp. 78 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.19.1.78 _zAvailable from publisher's website |
999 |
_c7069390 _d7069390 |