WordNet

tell the sex (of young chickens)
the properties that distinguish organisms on the basis of their reproductive roles; "she didnt want to know the sex of the foetus" (同)gender, sexuality
all of the feelings resulting from the urge to gratify sexual impulses; "he wanted a better sex life"; "the film contained no sex or violence" (同)sexual urge
either of the two categories (male or female) into which most organisms are divided; "the war between the sexes"
a change from one state to the opposite state; "there was a reversal of autonomic function"
a judgment by a higher court that the judgment of a lower court was incorrect and should be set aside
a decision to reverse an earlier decision (同)change of mind, flip-flop, turnabout, turnaround
turning in an opposite direction or position; "the reversal of the image in the lens" (同)turn_around
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
a lapel on a womans garment; turned back to show the reverse side (同)revere
having sexual differentiation
characterized by sexuality; "highly sexed"

PrepTutorEJDIC

〈U〉〈C〉『性』,性別 / 《the~》《形容詞を伴い集合的に》『男性』,『女性』 / 〈U〉(男女(雌雄)間の)相違[の意識] / 〈U〉性に関する事柄(情報) / 〈U〉性交 / 〈ひよこなど〉‘の'性別を見分ける
(…を)逆にすること,裏返すこと《+『of』+『名』》
(疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
（フランス語）(えりの)裏出し,折り返し

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1. 小児における原発性副腎不全の原因および臨床症状 causes and clinical manifestations of primary adrenal insufficiency in children
2. 非定型生殖器（性分化疾患）を有する乳児の評価 evaluation of the infant with atypical genitalia disorder of sex development
3. 微細欠失症候群（12番～22番染色体） microdeletion syndromes chromosomes 12 to 22
4. 副腎不全の稀な原因 unusual causes of adrenal insufficiency
5. 致死的骨格形成異常の出生前診断 prenatal diagnosis of the lethal skeletal dysplasias

Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis.

Fan BJ1, Pasquale LR2, Kang JH3, Levkovitch-Verbin H4, Haines JL5, Wiggs JL6.
Experimental eye research.Exp Eye Res.2015 Oct;139:115-22. doi: 10.1016/j.exer.2015.08.004. Epub 2015 Aug 10.
Exfoliation syndrome (XFS) is an important risk factor for glaucoma (XFG) worldwide. LOXL1 variants are highly associated with XFS in most populations; however, the high frequency of risk alleles in normal individuals and the reversal of risk alleles in different ethnic populations suggest that othe
PMID 26272660

Bagheri-Fam S1, Ono M2, Li L3, Zhao L4, Ryan J2, Lai R2, Katsura Y5, Rossello FJ6, Koopman P4, Scherer G7, Bartsch O8, Eswarakumar JV3, Harley VR1.
Human molecular genetics.Hum Mol Genet.2015 Sep 11. pii: ddv374. [Epub ahead of print]
Patients with 46,XY gonadal dysgenesis (GD) exhibit genital anomalies, which range from hypospadias to complete male-to-female sex reversal. However, a molecular diagnosis is made in only 30% of cases. Heterozygous mutations in the human FGFR2 gene cause various craniosynostosis syndromes including
PMID 26362256

A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures.

Smyk M1, Roeder E2, Cheung SW3, Szafranski P3, Stankiewicz P3.
American journal of medical genetics. Part A.Am J Med Genet A.2015 Aug;167(8):1842-50. doi: 10.1002/ajmg.a.37057. Epub 2015 Jun 8.
Defects of long-range regulatory elements of dosage-sensitive genes represent an under-recognized mechanism underlying genetic diseases. Haploinsufficiency of SOX9, the gene essential for development of testes and differentiation of chondrocytes, results in campomelic dysplasia, a skeletal malformat
PMID 26059046