Genetics, Birth Defects

Contributing journals to this collection:
AAP Grand Rounds, NeoReviews, Pediatrics, and Pediatrics in Review

Citations 41-50 of 219 total displayed.

Past content

Pediatrics
ARTICLES
Clinical and Genetic Analysis of Unclassifiable Inherited Bone Marrow Failure Syndromes
Juliana T. Teo, Robert Klaassen, Conrad V. Fernandez, Rochelle Yanofsky, John Wu, Josette Champagne, Mariana Silva, Jeffrey H. Lipton, Jossee Brossard, Yvan Samson, Sharon Abish, MacGregor Steele, Kaiser Ali, Uma Athale, Lawrence Jardine, John P. Hand, Elena Tsangaris, Isaac Odame, Joseph Beyene, and Yigal Dror
Pediatrics 2008; 122: e139-e148. [Abstract] [Full text] [PDF]  

Pediatr. Rev.
Articles
Turner Syndrome
Melissa L. Loscalzo
Pediatr. Rev. 2008; 29: 219-227. [Extract] [Full text] [PDF]  

NeoReviews
Articles
Advances in Genetic Testing and Applications in Newborn Medicine
Kara Goodin, Margaret Chen, Edward Lose, Fady M. Mikhail, and Bruce R. Korf
NeoReviews 2008; 9: e282-e290. [Abstract] [Full text] [PDF]  

NeoReviews
Articles
Testing Strategy for Inborn Errors of Metabolism in the Neonate
Aditi I. Dagli, Roberto T. Zori, and Bryce A. Heese
NeoReviews 2008; 9: e291-e298. [Abstract] [Full text] [PDF]  

NeoReviews
Articles
Neonatal Presentations of CHARGE Syndrome and VATER/VACTERL Association
Julie Kaplan and Louanne Hudgins
NeoReviews 2008; 9: e299-e304. [Abstract] [Full text] [PDF]  

Pediatrics
ARTICLES
Early Determinants of Fractures in Rett Syndrome
Jennepher Downs, Ami Bebbington, Helen Woodhead, Peter Jacoby, Le Jian, Amanda Jefferson, and Helen Leonard
Pediatrics 2008; 121: 540-546. [Abstract] [Full text] [PDF]  

Pediatrics
STATE-OF-THE-ART REVIEW ARTICLES
Ethical, Legal, and Social Concerns About Expanded Newborn Screening: Fragile X Syndrome as a Prototype for Emerging Issues
Donald B. Bailey, Jr, Debra Skinner, Arlene M. Davis, Ian Whitmarsh, and Cynthia Powell
Pediatrics 2008; 121: e693-e704. [Abstract] [Full text] [PDF]  

Pediatrics
EXPERIENCE & REASON
Successful Management of Difficult Infusion-Associated Reactions in a Young Patient With Mucopolysaccharidosis Type VI Receiving Recombinant Human Arylsulfatase B (Galsulfase [Naglazyme])
Katherine H. Kim, Celeste Decker, and Barbara K. Burton
Pediatrics 2008; 121: e714-e717. [Abstract] [Full text] [PDF]  

Pediatrics
EXPERIENCE & REASON
Successful Management of Difficult Infusion-Associated Reactions in a Young Patient With Mucopolysaccharidosis Type VI Receiving Recombinant Human Arylsulfatase B (Galsulfase [Naglazyme])
Katherine H. Kim, Celeste Decker, and Barbara K. Burton
Pediatrics peds.2007-0665. [Abstract] [Full text] [PDF]  

Pediatrics
REVIEW ARTICLES
Recognition and Diagnosis of Mucopolysaccharidosis II (Hunter Syndrome)
Rick Martin, Michael Beck, Christine Eng, Roberto Giugliani, Paul Harmatz, Verónica Muñoz, and Joseph Muenzer
Pediatrics 2008; 121: e377-e386. [Abstract] [Full text] [PDF]  

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