2004 May 21 [updated 2023 May 18]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301540
Fetal micromelia, thoracic dysplasia and polydactyly revisited: A case-based antenatal sonographic approach.
Agarwal A, Agarwal S.
Ultrasound. 2019 Aug;27(3):196-201. doi: 10.1177/1742271X19847223. Epub 2019 May 15.
PMID:32549900
Opsismodysplasia.
Lewis LE, Ramesh Bhat Y, Naik P, Sethi K, Girisha KM.
Indian J Pediatr. 2010 May;77(5):567-8. doi: 10.1007/s12098-010-0043-z. Epub 2010 Mar 19.
PMID:20422326
Further Delineation of the Microcephaly-Micromelia Syndrome Associated with Loss-of-Function Variants in DONSON.
Abdelrahman HA, John A, Ali BR, Al-Gazali L.
Mol Syndromol. 2019 May;10(3):171-176. doi: 10.1159/000497337. Epub 2019 Mar 6.
PMID:31191207
Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1.
Pace JM, Li Y, Seegmiller RE, Teuscher C, Taylor BA, Olsen BR.
Dev Dyn. 1997 Jan;208(1):25-33. doi: 10.1002/(SICI)1097-0177(199701)208:1<25::AID-AJA3>3.0.CO;2-3.
PMID:8989518
Loss of U11 small nuclear RNA in the developing mouse limb results in micromelia.
Development. 2020 Aug 14;147(21):dev190967. doi: 10.1242/dev.190967.
PMID:32665241
[MICROMELIA AND RUBELLA].
VAN CREVELD.
Arch Gesamte Virusforsch. 1965;16:392.
PMID:14322901
Sporadic Class II Congenital humeroradial synostosis and Left Micromelia in a three-and-a-half-months female Ghanaian infant.
Brakohiapa EK, Segbefia M, Nimo O, Sarkodie BD, Dzefi-Tettey K, Onimole E, Opoku M, Basogloyele C, Edzie EKM.
Radiol Case Rep. 2024 Feb 17;19(5):1797-1800. doi: 10.1016/j.radcr.2024.01.072. eCollection 2024 May.
PMID:38390430
An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomalies.
Verma IC, Bhargava S, Agarwal S.
Birth Defects Orig Artic Ser. 1975;11(6):167-74.
PMID:1103993
Spondyloenchondrodysplasia.
Menger H, Kruse K, Spranger J.
J Med Genet. 1989 Feb;26(2):93-9. doi: 10.1136/jmg.26.2.93.