000			01419 a2200433 4500
005			20250513041617.0
264		0	_c19950524
008			199505s 0 0 eng d
022			_a0002-9297
040			_aNLM _beng _cNLM
100	1		_aChurch, D M
245	0	0	_aMolecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features. _h[electronic resource]
260			_bAmerican journal of human genetics _cMay 1995
300			_a1162-72 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	_aBase Sequence
650	0	4	_aCells, Cultured
650	0	4	_aChromosome Deletion
650	0	4	_aChromosomes, Human, Pair 5 _xgenetics
650	0	4	_aCri-du-Chat Syndrome _xclassification
650	0	4	_aFemale
650	0	4	_aGenetic Markers
650	0	4	_aHaplotypes
650	0	4	_aHumans
650	0	4	_aIn Situ Hybridization, Fluorescence
650	0	4	_aInfant
650	0	4	_aInfant, Newborn
650	0	4	_aMale
650	0	4	_aMolecular Sequence Data
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aPolymerase Chain Reaction
650	0	4	_aSequence Deletion
700	1		_aBengtsson, U
700	1		_aNielsen, K V
700	1		_aWasmuth, J J
700	1		_aNiebuhr, E
773	0		_tAmerican journal of human genetics _gvol. 56 _gno. 5 _gp. 1162-72
999			_c7725541 _d7725541