Diagnosis and genetics of alacrima-Reference-Cited by-同舟云学术

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Diagnosis and genetics of alacrima

Published:2018-02-05 Issue:1 Volume:94 Page:54-60
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Adams J.¹,Schaaf C.P.²³

Affiliation:

1. Baylor College of Medicine; Interdepartmental Program of Developmental Biology; Houston TX

2. Baylor College of Medicine; Department of Molecular and Human Genetics; Houston TX

3. Jan and Dan Duncan Neurological Research Institute; Texas Children's Hospital; Houston TX

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13173/fullpdf

Reference38 articles.

1. Triple A syndrome: genotype-phenotype assessment;Prpic;Clin Genet,2003

2. Infantile achalasia associated with deficient tear production;Efrati;J Clin Gastroenterol,1985

3. Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction;Koehler;Am J Hum Genet,2013

4. Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24;Spring;Brain,2005

5. A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24;Kok;Am J Hum Genet,2003

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