Literature DB >> 14902764

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

P J WAARDENBURG.   

Abstract

Entities:  

Keywords:  EYEBROWS/abnormalities; EYELIDS/abnormalities; NOSE/abnormalities

Mesh：

Year:  1951        PMID： 14902764      PMCID： PMC1716407     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  2 in total

1.  Unilateral developmental anomalies in sisters.

Authors:  C W Cotterman; H F Falls
Journal:  Am J Hum Genet       Date:  1949-12       Impact factor: 11.025

2.  Some statistical problems posed by Waardenburg's data on dystopia canthorum and associated anomalies.

Authors:  C W COTTERMAN
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025
  2 in total
  134 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  Waardenburg's syndrome in a girl.

Authors:  M L Magotra; O P Katira; V R Anand
Journal:  Indian J Pediatr       Date:  1975-02       Impact factor: 1.967

3.  Probable loose linkage between the ABO locus and Waardenburg syndrome type I.

Authors:  S Arias; M Mota; A Yánez; M Bolivar
Journal:  Humangenetik       Date:  1975

Review 4.  PROFOUND CHILDHOOD DEAFNESS.

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

5.  WAARDENBURG'S SYNDROME: REPORT OF A PEDIGREE.

Authors:  A C HANSEN; G ACKAOUY; E P CRUMP
Journal:  J Natl Med Assoc       Date:  1965-01       Impact factor: 1.798

6.  A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance.

Authors:  W TIETZ
Journal:  Am J Hum Genet       Date:  1963-09       Impact factor: 11.025

7.  An English family with Waardenburg's syndrome.

Authors:  M W PARTINGTON
Journal:  Arch Dis Child       Date:  1959-04       Impact factor: 3.791

8.  Congenital deafness due to a sex-linked recessive gene.

Authors:  N PARKER
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

9.  Heritability and segregation analysis of deafness in U.S. Dalmatians.

Authors:  E J Cargill; T R Famula; G M Strain; K E Murphy
Journal:  Genetics       Date:  2004-03       Impact factor: 4.562

10.  Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.

Authors:  Nadege Bondurand; Florence Dastot-Le Moal; Laure Stanchina; Nathalie Collot; Viviane Baral; Sandrine Marlin; Tania Attie-Bitach; Irina Giurgea; Laurent Skopinski; William Reardon; Annick Toutain; Pierre Sarda; Anis Echaieb; Marilyn Lackmy-Port-Lis; Renaud Touraine; Jeanne Amiel; Michel Goossens; Veronique Pingault
Journal:  Am J Hum Genet       Date:  2007-10-22       Impact factor: 11.025
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