Familial 46,XX gonadal dysgenesis

scientific article published on 01 March 1981

Familial 46,XX gonadal dysgenesis is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S0015-0282(16)45378-1
P698PubMed publication ID7202756

P2093author name stringF A Aleem
P2860cites workAutoimmunity and ovarian failureQ33464697
The Sella Turcica in Primary End Organ FailureQ39884675
Gonadal dysgenesis in phenotypic female subjects. A review of eighty-seven cases, with cytogenetic studies in fifty-threeQ40064411
Turner's Syndrome and phenotypeQ44184312
Phenotypic and cytogenetic findings in eighty-two patients with ovarian failure--changing trendsQ44733153
Familial Syndrome of Streak Gonads and Normal Male Karyotype in Five Phenotypic FemalesQ45066596
Three Siblings with Premature Gonadal FailureQ57971901
A new syndrome of amenorrhae in association with hypergonadotropism and apparently normal ovarian follicular apparatusQ72392574
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectgonadal dysgenesisQ1332427
P304page(s)317-320
P577publication date1981-03-01
P1433published inFertility and SterilityQ15724525
P1476titleFamilial 46,XX gonadal dysgenesis
P478volume35

Reverse relations

cites work (P2860)
Q35560259Mechanisms of follicular dysfunction in 46,XX spontaneous premature ovarian failure
Q35889339The genetics of XX gonadal dysgenesis