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comp in Homo sapiensMus musculusRattus norvegicusAll 555 Gene records
GeneReviews® [Internet].
Adam MP, Feldman J, Mirzaa GM, et al., editors.
Seattle (WA): University of Washington, Seattle; 1993-2024.
GeneReviews by Title GeneReviews Advanced Search Help
COMP-Related Pseudoachondroplasia.
Briggs MD, Wright MJ. 2004 Aug 20 [Updated 2023 Nov 30].
Multiple Epiphyseal Dysplasia, Autosomal Dominant.
Briggs MD, Wright MJ, Mortier GR. 2003 Jan 8 [Updated 2019 Apr 25].
SLC26A2-Related Multiple Epiphyseal Dysplasia.
Unger S, Superti-Furga A. 2002 Aug 29 [Updated 2023 Jan 19].
Resources for Genetics Professionals — Genetic Disorders Caused by Nucleotide Repeat Expansions and Contractions.
Wallace SE, Bean LJH. 2017 Mar 14 [Updated 2022 Oct 20].
X-Linked Spondyloepiphyseal Dysplasia Tarda.
Tiller GE. 2001 Nov 1 [Updated 2023 Apr 6].
GNPTAB-Related Disorders.
Leroy JG, Cathey SS, Friez MJ. 2008 Aug 26 [Updated 2019 Aug 29].
Type II Collagen Disorders Overview.
Gregersen PA, Savarirayan R. 2019 Apr 25.
Congenital Central Hypoventilation Syndrome.
Weese-Mayer DE, Rand CM, Khaytin I, et al. 2004 Jan 28 [Updated 2021 Jan 28].
Autosomal Dominant Tubulointerstitial Kidney Disease – REN.
Živná M, Kidd K, Kmoch S, et al. 2011 Apr 5 [Updated 2020 Dec 10].
KCNT1-Related Epilepsy.
Gertler T, Bearden D, Bhattacharjee A, et al. 2018 Sep 20.
Schmid Metaphyseal Chondrodysplasia.
Richmond CM, Savarirayan R. 2019 Oct 21.
SCN3A-Related Neurodevelopmental Disorder.
Helbig KL, Goldberg EM. 2021 Jun 3 [Updated 2021 Nov 4].
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