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Page 1
Oral Rehabilitation of a Child with Hypohidrotic Ectodermal Dysplasia.
J Dent Child (Chic). 2019 Sep 15;86(3):158-163.
J Dent Child (Chic). 2019.
PMID: 31645258
Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature.
Laus AC, Baratela WA, Laureano LA, Santos SA, Huber J, Ramos ES, Rebelo CC, Squire JA, Martelli L.
Laus AC, et al. Among authors: huber j.
Am J Med Genet A. 2012 Apr;158A(4):821-7. doi: 10.1002/ajmg.a.32988. Epub 2012 Feb 21.
Am J Med Genet A. 2012.
PMID: 22354628
Review.
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Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.
Araujo LF, Molfetta GA, Vincenzi OC, Huber J, Teixeira LA, Ferraz VE, Silva WA Jr.
Araujo LF, et al. Among authors: huber j.
Int J Biol Markers. 2019 Mar;34(1):80-89. doi: 10.1177/1724600818814462. Epub 2019 Mar 11.
Int J Biol Markers. 2019.
PMID: 30852976
Free article.
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Velocardiofacial syndrome with a rare t(2;22).
Huber J, Rainho CA, Gomes MV, Santos SA, Ramos ES.
Huber J, et al.
Clin Dysmorphol. 2007 Jul;16(3):181-183. doi: 10.1097/MCD.0b013e3280fa81de.
Clin Dysmorphol. 2007.
PMID: 17551333
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