000 01521 a2200385 4500
005 20250516135041.0
264 0 _c20140416
008 201404s 0 0 eng d
022 _a1661-5433
024 7 _a10.1159/000346958
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSaranya, B
245 0 0 _aTranslocation t(X;11)(q22;q25) in a woman with premature ovarian failure.
_h[electronic resource]
260 _bSexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
_c2013
300 _a216-21 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aChromosome Banding
650 0 4 _aChromosomes, Human, Pair 11
_xgenetics
650 0 4 _aChromosomes, Human, X
_xgenetics
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIn Situ Hybridization, Fluorescence
650 0 4 _aKaryotyping
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aPrimary Ovarian Insufficiency
_xgenetics
650 0 4 _aTranslocation, Genetic
700 1 _aKavitha Devi, D
700 1 _aChandra, R S
700 1 _aJayashankar, M
700 1 _aSanthiya, S T
773 0 _tSexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
_gvol. 7
_gno. 4
_gp. 216-21
856 4 0 _uhttps://doi.org/10.1159/000346958
_zAvailable from publisher's website
999 _c22523107
_d22523107