000 | 01878 a2200589 4500 | ||
---|---|---|---|
005 | 20250515143304.0 | ||
264 | 0 | _c20090319 | |
008 | 200903s 0 0 eng d | ||
022 | _a0197-3851 | ||
024 | 7 |
_a10.1002/pd.2088 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aSimon-Bouy, Brigitte | |
245 | 0 | 0 |
_aHypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling. _h[electronic resource] |
260 |
_bPrenatal diagnosis _cNov 2008 |
||
300 |
_a993-8 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAlkaline Phosphatase _xgenetics |
650 | 0 | 4 |
_aBone and Bones _xembryology |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenes, Recessive |
650 | 0 | 4 |
_aGenetic Counseling _xmethods |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHypophosphatasia _xdiagnostic imaging |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aPregnancy |
650 | 0 | 4 | _aUltrasonography, Prenatal |
700 | 1 | _aTaillandier, Agnès | |
700 | 1 | _aFauvert, Delphine | |
700 | 1 | _aBrun-Heath, Isabelle | |
700 | 1 | _aSerre, Jean-Louis | |
700 | 1 | _aArmengod, Carmen G | |
700 | 1 | _aBialer, Martin G | |
700 | 1 | _aMathieu, Michèle | |
700 | 1 | _aCousin, Jacques | |
700 | 1 | _aChitayat, David | |
700 | 1 | _aLiebelt, Jan | |
700 | 1 | _aFeldman, Barbara | |
700 | 1 | _aGérard-Blanluet, Marion | |
700 | 1 | _aKörtge-Jung, Stefani | |
700 | 1 | _aKing, Cath | |
700 | 1 | _aLaivuori, Hannele | |
700 | 1 | _aLe Merrer, Martine | |
700 | 1 | _aMehta, Sarju | |
700 | 1 | _aJern, Christina | |
700 | 1 | _aSharif, Saba | |
700 | 1 | _aPrieur, Fabienne | |
700 | 1 | _aGillessen-Kaesbach, Gabriele | |
700 | 1 | _aZankl, Andreas | |
700 | 1 | _aMornet, Etienne | |
773 | 0 |
_tPrenatal diagnosis _gvol. 28 _gno. 11 _gp. 993-8 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/pd.2088 _zAvailable from publisher's website |
999 |
_c18389257 _d18389257 |