000 01406 a2200385 4500
005 20250513193655.0
264 0 _c19991210
008 199912s 0 0 eng d
022 _a0002-9297
024 7 _a10.1086/302606
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChrist, L A
245 0 0 _aChromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cNov 1999
300 _a1387-95 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aCells, Cultured
650 0 4 _aChromosome Breakage
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Artificial, Yeast
650 0 4 _aChromosomes, Human, Pair 9
_xgenetics
650 0 4 _aCraniofacial Abnormalities
_xgenetics
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aLeukocytes
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aSequence Tagged Sites
700 1 _aCrowe, C A
700 1 _aMicale, M A
700 1 _aConroy, J M
700 1 _aSchwartz, S
773 0 _tAmerican journal of human genetics
_gvol. 65
_gno. 5
_gp. 1387-95
856 4 0 _uhttps://doi.org/10.1086/302606
_zAvailable from publisher's website
999 _c10478306
_d10478306