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Page 1
Comprehensive evaluation of the child with intellectual disability or global developmental delays.
Pediatrics. 2014 Sep;134(3):e903-18. doi: 10.1542/peds.2014-1839.
Pediatrics. 2014.
PMID: 25157020
Free PMC article.
Review.
Health supervision for children with Marfan syndrome.
Tinkle BT, Saal HM; Committee on genetics.
Tinkle BT, et al.
Pediatrics. 2013 Oct;132(4):e1059-72. doi: 10.1542/peds.2013-2063. Epub 2013 Sep 30.
Pediatrics. 2013.
PMID: 24081994
Review.
Item in Clipboard
Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency.
McGregor TL, Berry SA, Dipple KM, Hamid R; COUNCIL ON GENETICS.
McGregor TL, et al.
Pediatrics. 2021 Jan;147(1):e2020040303. doi: 10.1542/peds.2020-040303.
Pediatrics. 2021.
PMID: 33372121
Item in Clipboard
Technical report: Ethical and policy issues in genetic testing and screening of children.
Ross LF, Saal HM, David KL, Anderson RR; American Academy of Pediatrics; American College of Medical Genetics and Genomics.
Ross LF, et al.
Genet Med. 2013 Mar;15(3):234-45. doi: 10.1038/gim.2012.176. Epub 2013 Feb 21.
Genet Med. 2013.
PMID: 23429433
Free article.
Item in Clipboard
Development, testing, and validation of a patient satisfaction questionnaire for use in the clinical genetics setting.
Zellerino B, Milligan SA, Brooks R, Freedenberg DL, Collingridge DS, Williams MS.
Zellerino B, et al. Among authors: freedenberg dl.
Am J Med Genet C Semin Med Genet. 2009 Aug 15;151C(3):191-9. doi: 10.1002/ajmg.c.30214.
Am J Med Genet C Semin Med Genet. 2009.
PMID: 19621441
Item in Clipboard
MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection.
Freedenberg DL, Chen SH, Kurachi K, Scott CR.
Freedenberg DL, et al.
Hum Genet. 1987 Jul;76(3):262-4. doi: 10.1007/BF00283620.
Hum Genet. 1987.
PMID: 2439437
Free article.
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Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development.
Freedenberg DL, Gane LW, Richards CS, Lampe M, Hills J, O'Connor R, Manchester D, Taylor A, Tassone F, Hulseberg D, Hagerman RJ, Patil SR.
Freedenberg DL, et al.
Am J Med Genet. 1999 Jul 30;85(3):197-201. doi: 10.1002/(sici)1096-8628(19990730)85:3<197::aid-ajmg1>3.0.co;2-o.
Am J Med Genet. 1999.
PMID: 10398226
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