000 01242 a2200421 4500
005 20250511175352.0
264 0 _c19930422
008 199304s 0 0 eng d
022 _a0003-3995
040 _aNLM
_beng
_cNLM
100 1 _aStoppoloni, G
245 0 0 _aSeckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locus.
_h[electronic resource]
260 _bAnnales de genetique
_c1992
300 _a213-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChild
650 0 4 _aDwarfism
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Linkage
650 0 4 _aHLA Antigens
_xgenetics
650 0 4 _aHaplotypes
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aPuberty, Precocious
_xgenetics
650 0 4 _aSyndrome
700 1 _aStabile, M
700 1 _aRinaldi, M M
700 1 _aPrisco, F
700 1 _aRabuano, R G
700 1 _aPace, E
700 1 _aIafusco, D
700 1 _aStoppoloni, F
700 1 _aGreco, N
773 0 _tAnnales de genetique
_gvol. 35
_gno. 4
_gp. 213-6
999 _c1303043
_d1303043