A Unique Case of Facial Dysmorphism in an Infant-Reference-Cited by-同舟云学术

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A Unique Case of Facial Dysmorphism in an Infant

Published:2018-02-01 Issue:2 Volume:19 Page:e127-e129
ISSN:1526-9906
Container-title:NeoReviews
language:en
Short-container-title:

Author:

Samuel Sharmeen¹,Karpawich Peter P.²,Scheurer-Monaghan Andrea³

Affiliation:

1. Department of Pediatrics, Western Michigan University, Homer Stryker M.D. School of Medicine, Kalamazoo, MI

2. Department of Pediatric Cardiology, Children’s Hospital of Michigan/Wayne State University, Detroit, MI

3. Department of Neonatology, Bronson Methodist Hospital/Western Michigan University, Kalamazoo, MI

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Link

https://publications.aap.org/neoreviews/article-pdf/19/2/e127/829853/neoreviews_02samuel.pdf

Reference10 articles.

1. Stallings RL, Doggett NA. What’s different about Chromosome 16? Los Alamos Sci. 1992;20:211–215. Available at: https://fas.org/sgp/othergov/doe/lanl/pubs/00326708.pdf. Accessed November 9, 2017

2. Molecular studies of non-disjunction in trisomy 16;Hassold;J Med Genet,1991

3. Increased chromosome 16 disomy rates in human spermatozoa and recurrent spontaneous abortions;Neusser;Fertil Steril,2015

4. Trisomy 16 and trisomy 16 mosaicism: a review;Benn;Am J Med Genet,1998

5. Mosaic trisomy 16 in a live newborn infant;Gilbertson;Arch Dis Child,1990

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