Literature DB >> 13584032

The first arch syndrome.

J McKENZIE.   

Abstract

Entities:  

Keywords:  BRANCHIAL REGION/abnormalities

Mesh：

Year:  1958        PMID： 13584032      PMCID： PMC2012316          DOI： 10.1136/adc.33.171.477

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  8 in total

1.  Multiple congenital abnormalities in the rat resulting from riboflavin deficiency induced by the antimetabolite galactoflavin.

Authors:  M M NELSON; C D BAIRD; H V WRIGHT; H M EVANS
Journal:  J Nutr       Date:  1956-01-10       Impact factor: 4.798

2.  Effects of irradiation of embryonic development. II. X-rays on the ninth day of gestation in the rat.

Authors:  J G WILSON; H C JORDAN; R L BRENT
Journal:  Am J Anat       Date:  1953-01

3.  Some effects on a maternal riboflavin deficiency on reproduction in the rat.

Authors:  J P W GILMAN; F A PERRY; D C HILL
Journal:  Can J Med Sci       Date:  1952-10

4.  Production of multiple congenital abnormalities in young by maternal pteroylglutamic acid deficiency during gestation.

Authors:  M M NELSON; C W ASLING; H M EVANS
Journal:  J Nutr       Date:  1952-09       Impact factor: 4.798

5.  Variations Coincident with Congenital Absence of the Zygoma (Zygomatic Process of Temporal Bone).

Authors:  R D Lockhart
Journal:  J Anat       Date:  1929-01       Impact factor: 2.610

6.  The Development of the External Ear.

Authors:  F Wood-Jones; W I-Chuan
Journal:  J Anat       Date:  1934-07       Impact factor: 2.610

7.  DEFICIENCY OF THE MALAR BONES WITH DEFECT OF THE LOWER LIDS: With Notes of a Similar Case, Treatment and Suggestions.

Authors:  I Mann; T P Kilner
Journal:  Br J Ophthalmol       Date:  1943-01       Impact factor: 4.638

8.  Therapeutic abortions with a folic acid antagonist, 4-aminopteroylglutamic acid (4-amino P.G.A) administered by the oral route.

Authors:  J B THIERSCH
Journal:  Am J Obstet Gynecol       Date:  1952-06       Impact factor: 8.661
  8 in total
  25 in total

1.  Goldenhar syndrome with rare associations.

Authors:  R Kumar; B Balani; A K Patwari; V K Anand; B Ahuja
Journal:  Indian J Pediatr       Date:  2000-03       Impact factor: 1.967

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.  Goldenhar's syndrome.

Authors:  G Gathwala; A D Tiwari; I Singh; S P Yadav
Journal:  Indian J Pediatr       Date:  1992 Nov-Dec       Impact factor: 1.967

Review 4.  PROFOUND CHILDHOOD DEAFNESS.

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

5.  An English family with Waardenburg's syndrome.

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

6.  Aplasia of the right lung and calcifying epithelioma in association with Goldenhar's syndrome.

Authors:  M M Kenawi; J A Dickson
Journal:  Postgrad Med J       Date:  1976-05       Impact factor: 2.401

7.  Pierre Robin syndrome: autosomal dominant inheritance with pleiotropic effect.

Authors:  S S Sidhu; R N Deshmukh
Journal:  Indian J Pediatr       Date:  1989 May-Jun       Impact factor: 1.967

8.  Goldenhar syndrome (oculo-auriculo-vertebral dysplasia) in a twin new born baby.

Authors:  M M Faridi; S Ahmad; R Moonis; Z Ansari; S K Bhargava
Journal:  Indian J Pediatr       Date:  1986 Mar-Apr       Impact factor: 1.967

9.  Orofacial malformations.

Authors:  D E Poswillo
Journal:  Proc R Soc Med       Date:  1974-05

10.  Goldenhar's syndrome.

Authors:  I Nessim-Morcos; M B Mathalone; I Kessel
Journal:  Br Med J       Date:  1968-02-24
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