000 01452 a2200433 4500
005 20250512010622.0
264 0 _c19900123
008 199001s 0 0 eng d
022 _a0148-7299
024 7 _a10.1002/ajmg.1320330415
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aZhu, D P
245 0 0 _aMicrodeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease.
_h[electronic resource]
260 _bAmerican journal of medical genetics
_cAug 1989
300 _a485-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aBlindness
_xetiology
650 0 4 _aBlotting, Southern
650 0 4 _aChromosome Deletion
650 0 4 _aDNA Probes
650 0 4 _aFemale
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
650 0 4 _aRestriction Mapping
650 0 4 _aRetina
_xabnormalities
650 0 4 _aX Chromosome
700 1 _aAntonarakis, S E
700 1 _aSchmeckpeper, B J
700 1 _aDiergaarde, P J
700 1 _aGreb, A E
700 1 _aMaumenee, I H
773 0 _tAmerican journal of medical genetics
_gvol. 33
_gno. 4
_gp. 485-8
856 4 0 _uhttps://doi.org/10.1002/ajmg.1320330415
_zAvailable from publisher's website
999 _c2602407
_d2602407