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