Diagnosis and Management of Infertility: A Review.
Carson SA, Kallen AN.
JAMA. 2021 Jul 6;326(1):65-76. doi: 10.1001/jama.2021.4788.
Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive form.
Meyers CM, Boughman JA, Rivas M, Wilroy RS, Simpson JL.
Am J Med Genet. 1996 Jun 28;63(4):518-24. doi: 10.1002/(SICI)1096-8628(19960628)63:4<518::AID-AJMG2>3.0.CO;2-K.
Genetics of primary ovarian insufficiency.
Rossetti R, Ferrari I, Bonomi M, Persani L.
Clin Genet. 2017 Feb;91(2):183-198. doi: 10.1111/cge.12921. Epub 2016 Dec 12.
Routine 36-week scan: diagnosis of fetal abnormalities.
Syngelaki A, Mitsigiorgi R, Goadsby J, Hamed K, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol. 2025 Apr;65(4):427-435. doi: 10.1002/uog.29218. Epub 2025 Mar 25.
[Ovarian dysgenesis].
FOSSATI P.
Lille Med. 1962 Mar;7:273-9.
[Ovarian dysgenesis].
[No authors listed]
Annee Endocrinol. 1957;9:136-51.
[SF-1, a key player in adrenal and gonadal differentiation: implications in gonadal dysgenesis and primary ovarian insufficiency].
Martinerie L, Bouvattier C, Lombes M.
Ann Endocrinol (Paris). 2009 Sep;70 Suppl 1:S26-32. doi: 10.1016/S0003-4266(09)72473-4.
Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.
Narahara K, Kamada M, Takahashi Y, Tsuji K, Yokoyama Y, Ninomiya S, Seino Y.
Am J Med Genet. 1992 Oct 1;44(3):369-73. doi: 10.1002/ajmg.1320440320.
Turner Syndrome and Fertility.
Viuff M, Gravholt CH.
Ann Endocrinol (Paris). 2022 Aug;83(4):244-249. doi: 10.1016/j.ando.2022.06.001. Epub 2022 Jun 18.
Ovarian dysgenesis in individuals with chromosomal abnormalities.
Cunniff C, Jones KL, Benirschke K.
Hum Genet. 1991 Apr;86(6):552-6. doi: 10.1007/BF00201540.
