| 000 | 01425 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250514000134.0 | ||
| 264 | 0 | _c20010927 | |
| 008 | 200109s 0 0 eng d | ||
| 022 | _a1098-3600 | ||
| 024 | 7 |
_a10.1097/00125817-200101000-00004 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDriscoll, D A | |
| 245 | 0 | 0 |
_aPrenatal diagnosis of the 22q11.2 deletion syndrome. _h[electronic resource] |
| 260 |
_bGenetics in medicine : official journal of the American College of Medical Genetics _c |
||
| 300 |
_a14-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review | ||
| 650 | 0 | 4 | _aAbnormalities, Multiple |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 22 |
| 650 | 0 | 4 |
_aDiGeorge Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aFacies |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aGenetic Counseling |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIn Situ Hybridization, Fluorescence _xmethods |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPolymerase Chain Reaction _xmethods |
| 650 | 0 | 4 | _aPrenatal Diagnosis |
| 650 | 0 | 4 | _aRisk Factors |
| 650 | 0 | 4 | _aSyndrome |
| 773 | 0 |
_tGenetics in medicine : official journal of the American College of Medical Genetics _gvol. 3 _gno. 1 _gp. 14-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1097/00125817-200101000-00004 _zAvailable from publisher's website |
| 999 |
_c11272388 _d11272388 |
||