000 | 01482 a2200457 4500 | ||
---|---|---|---|
005 | 20250513130301.0 | ||
264 | 0 | _c19971119 | |
008 | 199711s 0 0 eng d | ||
022 | _a0340-6717 | ||
024 | 7 |
_a10.1007/s004390050571 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBartsch, O | |
245 | 0 | 0 |
_aA large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region. _h[electronic resource] |
260 |
_bHuman genetics _cOct 1997 |
||
300 |
_a669-75 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosomes, Human, Pair 18 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 21 _xgenetics |
650 | 0 | 4 |
_aDown Syndrome _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aTelomere |
650 | 0 | 4 |
_aTranslocation, Genetic _xgenetics |
700 | 1 | _aHinkel, G K | |
700 | 1 | _aPetersen, M B | |
700 | 1 | _aKönig, U | |
700 | 1 | _aBugge, M | |
700 | 1 | _aMikkelsen, M | |
700 | 1 | _aAvramopoulos, D | |
700 | 1 | _aMorris, M | |
700 | 1 | _aAntonarakis, S E | |
773 | 0 |
_tHuman genetics _gvol. 100 _gno. 5-6 _gp. 669-75 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1007/s004390050571 _zAvailable from publisher's website |
999 |
_c9313187 _d9313187 |