Myhre syndrome: Clinical features and restrictive cardiopulmonary complications-Reference-Cited by-同舟云学术

Myhre syndrome: Clinical features and restrictive cardiopulmonary complications

Published:2015-09-30 Issue:12 Volume:167 Page:2893-2901
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Starr Lois J.¹²,Grange Dorothy K.³,Delaney Jeffrey W.⁴,Yetman Anji T.⁴,Hammel James M.⁵,Sanmann Jennifer N.²,Perry Deborah A.⁶,Schaefer G. Bradley⁷,Olney Ann Haskins¹

Affiliation:

1. Division of Clinical Genetics; University of Nebraska Medical Center; Munroe-Meyer Institute for Genetics and Rehabilitation; Omaha Nebraska

2. University of Nebraska Medical Center; Munroe-Meyer Institute for Genetics and Rehabilitation; Human Genetics Laboratory; Omaha Nebraska

3. Department of Pediatrics; Division of Genetics and Genomic Medicine; Washington University School of Medicine; St. Louis Missouri

4. Division of Cardiology; Children's Hospital and Medical Center; Omaha Nebraska

5. Division of Cardiac Surgery; Children's Hospital and Medical Center; Omaha Nebraska

6. Division of Pediatric Pathology; Children's Hospital and Medical Center; Omaha Nebraska

7. Division of Medical Genetics; Arkansas Children's Hospital; Little Rock Arkansas

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37273/fullpdf

Reference27 articles.

1. Retinal involvement in two unrelated patients with Myhre syndrome;Al Ageeli;Euro J Med Genet,2012

2. First Case of a Japanese girl with Myhre syndrome due to a heterozygous SMAD4 mutation;Asakura;Am J Med Genet Part A,2012

3. Myhre syndrome with ataxia and cerebellar atrophy;Bachmann-Gagescu;Clin Dysmorph,2011

4. Myhre syndrome: New reports, review, and differential diagnosis;Burglen;J Med Genet,2003

5. A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome;Caputo;Am J Hum Genet,2012

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