11bc662f36e84395bdfb111d4bc655ea51d02f8a
lrnassar
  Wed Oct 16 12:56:47 2024 -0700
Ordering the references, feedback from CR. Refs #34624

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 </p>
 
 <h2>References</h2>
 
 <p>
 Rehm HL, Berg JS, Brooks LD, Bustamante CD, Evans JP, Landrum MJ, Ledbetter DH, Maglott DR, Martin
 CL, Nussbaum RL <em>et al</em>.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/26014595" target="_blank">
 ClinGen--the Clinical Genome Resource</a>.
 <em>N Engl J Med</em>. 2015 Jun 4;372(23):2235-42.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/26014595" target="_blank">26014595</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474187/" target="_blank">PMC4474187</a>
 </p>
 
 <p>
+Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E
+<em>et al</em>.
+<a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(21)03031-8" target="_blank">
+Standards and guidelines for the interpretation of sequence variants: a joint consensus
+recommendation of the American College of Medical Genetics and Genomics and the Association for
+Molecular Pathology</a>.
+<em>Genet Med</em>. 2015 May;17(5):405-24.
+PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/25741868" target="_blank">25741868</a>; PMC: <a
+href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544753/" target="_blank">PMC4544753</a>
+</p>
+
+ <p>
 Riggs ER, Church DM, Hanson K, Horner VL, Kaminsky EB, Kuhn RM, Wain KE, Williams ES, Aradhya S,
 Kearney HM <em>et al</em>.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/22097934" target="_blank">
 Towards an evidence-based process for the clinical interpretation of copy number variation</a>.
 <em>Clin Genet</em>. 2012 May;81(5):403-12.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/22097934" target="_blank">22097934</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008023/" target="_blank">PMC5008023</a>
 </p>
 
 <p>
 Strande NT, Riggs ER, Buchanan AH, Ceyhan-Birsoy O, DiStefano M, Dwight SS, Goldstein J, Ghosh R,
 Seifert BA, Sneddon TP <em>et al</em>.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/28552198" target="_blank">
 Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed
 by the Clinical Genome Resource</a>.
 <em>Am J Hum Genet</em>. 2017 Jun 1;100(6):895-906.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/28552198" target="_blank">28552198</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473734/" target="_blank">PMC5473734</a>
 </p>
 
-<p>
-Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E
-<em>et al</em>.
-<a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(21)03031-8" target="_blank">
-Standards and guidelines for the interpretation of sequence variants: a joint consensus
-recommendation of the American College of Medical Genetics and Genomics and the Association for
-Molecular Pathology</a>.
-<em>Genet Med</em>. 2015 May;17(5):405-24.
-PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/25741868" target="_blank">25741868</a>; PMC: <a
-href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544753/" target="_blank">PMC4544753</a>
-</p>