Genetics, Birth Defects

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

Citations 101-110 of 219 total displayed.

Past content

ARTICLES
Clinical Characteristics and Natural History of Freeman-Sheldon Syndrome

David A. Stevenson, John C. Carey, Janice Palumbos, Ann Rutherford, Joyce Dolcourt, and Michael J. Bamshad
Pediatrics 2006; 117: 754-762. [Abstract] [Full text] [PDF]  

EXPERIENCE AND REASON
Prenatal Diagnosis of Familial Type I Choledochal Cyst

Matthew S. Clifton, Ruth B. Goldstein, Anne Slavotinek, Mary E. Norton, Hanmin Lee, Jody Farrell, and Kerilyn K. Nobuhara
Pediatrics peds.2005-1411. [Abstract] [Full text] [PDF]  

HEMATOLOGY AND ONCOLOGY
Genetic Polymorphisms Influence ALL Outcome

Anthony Villella
AAP Grand Rounds 2005; 14: 63. [Extract] [Full text] [PDF]  

ARTICLE
Initially Misleading Communication of Carrier Results After Newborn Genetic Screening

Alison La Pean and Michael H. Farrell
Pediatrics 2005; 116: 1499-1505. [Abstract] [Full text] [PDF]  

ELECTRONIC ARTICLE
Complete DiGeorge Anomaly in the Absence of Neonatal Hypocalcemia and Velofacial and Cardiac Defects

Salem Al-Tamemi, Bruce Mazer, David Mitchell, Pedro Albuquerque, Alessandra M. V. Duncan, Christine McCusker, and Nada Jabado
Pediatrics 2005; 116: e457-e460. [Abstract] [Full text] [PDF]  

ELECTRONIC ARTICLE
Multiple Endocrine Neoplasia Type 2A in a Kindred With C634Y Mutation

Malaka B. Jackson, Marta Guttenberg, Holly Hedrick, and Thomas Moshang, Jr
Pediatrics 2005; 116: e468-e471. [Abstract] [Full text] [PDF]  

ARTICLE
Decline in the Prevalence of Spina Bifida and Anencephaly by Race/Ethnicity: 1995–2002

Laura J. Williams, Sonja A. Rasmussen, Alina Flores, Russell S. Kirby, and Larry D. Edmonds
Pediatrics 2005; 116: 580-586. [Abstract] [Full text] [PDF]  

AMERICAN ACADEMY OF PEDIATRICS
Health Supervision for Children With Achondroplasia

Tracy L. Trotter, Judith G. Hall and the Committee on Genetics
Pediatrics 2005; 116: 771-783. [Abstract] [Full text] [PDF]  

EXPERIENCE_AND_REASON
Multiple Endocrine Neoplasia Type 2A in a Kindred With C634Y Mutation

Malaka B. Jackson, Marta Guttenberg, Holly Hedrick, and Thomas Moshang
Pediatrics peds.2005-0033. [Abstract] [Full text] [PDF]  

EXPERIENCE_AND_REASON
Complete DiGeorge Anomaly in the Absence of Neonatal Hypocalcemia and Velofacial and Cardiac Defects

Salem Al-Tamemi, Bruce Mazer, David Mitchell, Pedro Albuquerque, Alessandra M. V. Duncan, Christine McCusker, and Nada Jabado
Pediatrics peds.2005-0371. [Abstract] [Full text] [PDF]  

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