Genetics, Birth Defects

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

Citations 201-210 of 219 total displayed.

Past content

EXPERIENCE AND REASON
Advance Directives in a Pediatric Emergency Department

Christine M. Walsh-Kelly, Kellie R. Lang, Jane Chevako, Ellen L. Blank, Nancy Korom, Kristi Kirk, and Amanda Gray
Pediatrics 1999; 103: 826-830. [Abstract] [Full text] [PDF]  

ARTICLE
Utilization and Perceptions of Genetics Services

Lawrence R. Shapiro
AAP Grand Rounds 1999; 1: 10-a-11-a. [Extract] [Full text] [PDF]  

Articles
Consultation with the Specialist: Pediatric Approach to Craniosynostosis

Gregory S. Liptak and Joseph M. Serletti
Pediatr. Rev. 1998; 19: 352-359. [Extract] [Full text] [PDF]  

ELECTRONIC ARTICLE
Who Gets Missed: Coverage in a Provincial Newborn Screening Program for Metabolic Disease

Donald W. Spady, L. Duncan Saunders, and Fiona Bamforth
Pediatrics 1998; 102: e21. [Abstract] [Full text] [PDF]  

COMMENTARY
Physician's Duty to Warn Third Parties About the Risk of Genetic Diseases

Gary N. McAbee, Jack Sherman, and Barbara Davidoff-Feldman
Pediatrics 1998; 102: 140-141. [Extract] [Full text] [PDF]  

EXPERIENCE AND REASON
Point Mutation in Exon 12 of the Receptor Tyrosine Kinase Proto-oncogene RET in Ondine-Hirschsprung Syndrome

Tetsuo Sakai, Akira Wakizaka, Hiroo Matsuda, Yuji Nirasawa, and Yasuo Itoh
Pediatrics 1998; 101: 924-925. [Abstract] [Full text] [PDF]  

ARTICLE
Prevalence of IgA-Antigliadin Antibodies and IgA-Antiendomysium Antibodies Related to Celiac Disease in Children With Down Syndrome

Annelie Carlsson, Irené Axelsson, Stefan Borulf, Anders Bredberg, Marianne Forslund, Bengt Lindberg, Klas Sjöberg, and Sten-Anders Ivarsson
Pediatrics 1998; 101: 272-275. [Abstract] [Full text] [PDF]  

EXPERIENCE AND REASON
Thalamic Syndrome in Children With Measles Infection and Selective, Reversible Thalamic Involvement

Martino Ruggieri, Agata Polizzi, Lorenzo Pavone, and Salvatore Musumeci
Pediatrics 1998; 101: 112. [Extract] [Full text] [PDF]  

ELECTRONIC ARTICLE
Lack of Deafness in Crigler-Najjar Syndrome Type 1: A Patient Survey

Gautham Suresh and Jerold F. Lucey
Pediatrics 1997; 100: e9. [Abstract] [Full text] [PDF]  

ARTICLE
Endocrinologic Disorders and Optic Pathway Gliomas in Children With Neurofibromatosis Type 1

Marjon H. Cnossen, Esther N. Stam, Linda C. M. G. Cooiman, Huibert J. Simonsz, Hans Stroink, Arnold P. Oranje, Dicky J. J. Halley, Arja de Goede-Bolder, Martinus F. Niermeijer, and Sabine M. P. F. de Muinck Keizer-Schrama
Pediatrics 1997; 100: 667-670. [Abstract] [Full text] [PDF]  

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