Rubella.
Winter AK, Moss WJ.
Lancet. 2022 Apr 2;399(10332):1336-1346. doi: 10.1016/S0140-6736(21)02691-X.
Rubella (German measles) revisited.
Leung AKC, Hon KL, Leong KF.
Hong Kong Med J. 2019 Apr;25(2):134-141. doi: 10.12809/hkmj187785. Epub 2019 Apr 10.
Myotonic Dystrophy Type 1.
Bird TD.
1999 Sep 17 [updated 2024 Nov 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Smith-Lemli-Opitz Syndrome.
Nowaczyk MJM, Wassif CA.
1998 Nov 13 [updated 2020 Jan 30]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Branchiooculofacial Syndrome.
Lin AE, Haldeman-Englert CR, Milunsky JM.
2011 May 31 [updated 2023 Sep 28]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Secondary congenital aphakia.
Ionescu C, Dascalescu D, Cristea M, Schmitzer S, Cioboata M, Iancu R, Corbu C.
Rom J Ophthalmol. 2016 Jan-Mar;60(1):37-9.
Aymé-Gripp Syndrome.
Amudhavalli SM, Gadea R, Gripp K.
2020 Feb 6. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Connexin Mutations and Hereditary Diseases.
Qiu Y, Zheng J, Chen S, Sun Y.
Int J Mol Sci. 2022 Apr 12;23(8):4255. doi: 10.3390/ijms23084255.
Congenital rubella.
Dudgeon JA.
J Pediatr. 1975 Dec;87(6 Pt 2):1078-86. doi: 10.1016/s0022-3476(75)80119-3.
[Hereditary peroxisomal diseases].
Astudillo L, Sabourdy F, Touati G, Levade T.
Presse Med. 2016 Mar;45(3):302-12. doi: 10.1016/j.lpm.2015.05.009. Epub 2016 Feb 18.
