000 01621 a2200445 4500
005 20250514204834.0
264 0 _c20050302
008 200503s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.30269
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOunap, K
245 0 0 _aThree patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cNov 2004
300 _a415-23 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 9
_xgenetics
650 0 4 _aChromosomes, Human, X
_xgenetics
650 0 4 _aChromosomes, Human, Y
_xgenetics
650 0 4 _aDNA-Binding Proteins
_xgenetics
650 0 4 _aDisorders of Sex Development
650 0 4 _aFemale
650 0 4 _aGrowth Disorders
_xgenetics
650 0 4 _aHumans
650 0 4 _aMonosomy
650 0 4 _aPuberty
650 0 4 _aSex Chromosome Aberrations
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aUibo, O
700 1 _aZordania, R
700 1 _aKiho, L
700 1 _aIlus, T
700 1 _aOiglane-Shlik, E
700 1 _aBartsch, O
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 130A
_gno. 4
_gp. 415-23
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.30269
_zAvailable from publisher's website
999 _c15171830
_d15171830