| 000 | 01577 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250516144452.0 | ||
| 264 | 0 | _c20140305 | |
| 008 | 201403s 0 0 eng d | ||
| 022 | _a1432-1203 | ||
| 024 | 7 |
_a10.1007/s00439-013-1304-5 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMcElroy, Jude J | |
| 245 | 0 | 0 |
_aMaternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. _h[electronic resource] |
| 260 |
_bHuman genetics _cAug 2013 |
||
| 300 |
_a935-42 p. _bdigital |
||
| 500 | _aPublication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 |
_aCodon _xgenetics |
| 650 | 0 | 4 |
_aExome _xgenetics |
| 650 | 0 | 4 | _aFamily |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFinland |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPolymorphism, Single Nucleotide _xgenetics |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aPremature Birth _xgenetics |
| 650 | 0 | 4 |
_aReceptors, Complement _xgenetics |
| 650 | 0 | 4 | _aSignal Transduction |
| 700 | 1 | _aGutman, Courtney E | |
| 700 | 1 | _aShaffer, Christian M | |
| 700 | 1 | _aBusch, Tamara D | |
| 700 | 1 | _aPuttonen, Hilkka | |
| 700 | 1 | _aTeramo, Kari | |
| 700 | 1 | _aMurray, Jeffrey C | |
| 700 | 1 | _aHallman, Mikko | |
| 700 | 1 | _aMuglia, Louis J | |
| 773 | 0 |
_tHuman genetics _gvol. 132 _gno. 8 _gp. 935-42 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-013-1304-5 _zAvailable from publisher's website |
| 999 |
_c22674677 _d22674677 |
||