| 000 | 01614 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250514011314.0 | ||
| 264 | 0 | _c20011025 | |
| 008 | 200110s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/ajmg.1509 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAl-Gazali, L I | |
| 245 | 0 | 0 |
_aAbnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cOct 2001 |
||
| 300 |
_a128-32 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAmino Acids, Sulfur _xblood |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aDNA Methylation |
| 650 | 0 | 4 |
_aDown Syndrome _xenzymology |
| 650 | 0 | 4 |
_aFolic Acid _xmetabolism |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMethylenetetrahydrofolate Reductase (NADPH2) |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNeural Tube Defects _xenzymology |
| 650 | 0 | 4 |
_aOxidoreductases Acting on CH-NH Group Donors _xgenetics |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 700 | 1 | _aPadmanabhan, R | |
| 700 | 1 | _aMelnyk, S | |
| 700 | 1 | _aYi, P | |
| 700 | 1 | _aPogribny, I P | |
| 700 | 1 | _aPogribna, M | |
| 700 | 1 | _aBakir, M | |
| 700 | 1 | _aHamid, Z A | |
| 700 | 1 | _aAbdulrazzaq, Y | |
| 700 | 1 | _aDawodu, A | |
| 700 | 1 | _aJames, S J | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 103 _gno. 2 _gp. 128-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.1509 _zAvailable from publisher's website |
| 999 |
_c11490795 _d11490795 |
||