Literature DB >> 4774830

Hirschsprung's disease and congenital deafness.

R Skinner, D Irvine.   

Abstract

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Year:  1973        PMID： 4774830      PMCID： PMC1013052          DOI： 10.1136/jmg.10.4.337

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

Authors:  G R FRASER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

2.  Deafness as part of an hereditary syndrome.

Authors:  L FISCH
Journal:  J Laryngol Otol       Date:  1959-06       Impact factor: 1.469

3.  The origin of intrinsic ganglia of trunk viscera from vagal neural crest in the chick embryo.

Authors:  C L YNTEMA; W S HAMMOND
Journal:  J Comp Neurol       Date:  1954-10       Impact factor: 3.215

4.  The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.

Authors:  E Passarge
Journal:  N Engl J Med       Date:  1967-01-19       Impact factor: 91.245
  4 in total
  5 in total

1.  Letter: Hirschsprung's disease and congenital deafness.

Authors:  R B Lowry
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Hirschsprung's disease and congenital deafness. Familial assocation.

Authors:  A G Weinberg; G Currarino; A M Besserman
Journal:  Hum Genet       Date:  1977-09-22       Impact factor: 4.132

3.  Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.

Authors:  H Santos; J Mateus; M J Leal
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

4.  USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.

Authors:  Thomas J Jaworek; Rashid Bhatti; Noreen Latief; Shaheen N Khan; Saima Riazuddin; Zubair M Ahmed
Journal:  J Hum Genet       Date:  2012-06-21       Impact factor: 3.172

5.  A prospective observational study of associated anomalies in Hirschsprung's disease.

Authors:  Alessio Pini Prato; Valentina Rossi; Manuela Mosconi; Catarina Holm; Francesca Lantieri; Paola Griseri; Isabella Ceccherini; Domenico Mavilio; Vincenzo Jasonni; Giulia Tuo; Maria Derchi; Maurizio Marasini; Gianmichele Magnano; Claudio Granata; Gianmarco Ghiggeri; Enrico Priolo; Lorenza Sposetti; Adelina Porcu; Piero Buffa; Girolamo Mattioli
Journal:  Orphanet J Rare Dis       Date:  2013-11-23       Impact factor: 4.123
  5 in total

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