Literature DB >> 13928435

Arhinencephaly.

J W LANDAU, J M BARRY, R KOCH.   

Abstract

Entities:  

Keywords:  MONSTERS

Mesh：

Year:  1963        PMID： 13928435     DOI： 10.1016/s0022-3476(63)80104-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  7 in total

1.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

2.  Arrhinencephaly associated with a deficiency involving chromosome 18.

Authors:  A McDermott; J Insley; M E Barton; P Roowe; J H Edwards; A H Cameron
Journal:  J Med Genet       Date:  1968-03       Impact factor: 6.318

3.  Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Authors:  P Fischer; E Golob; F Friedrich; E Kunze-Mühl; W Doleschel; H Aichmair
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

4.  What is the incidence of holoprosencephaly?

Authors:  E S Saunders; D Shortland; P M Dunn
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

5.  Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.

Authors:  N Fitch; H Srolovitz; Y Robitaille; F Guttman
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

6.  Eyes in arhinencephalic syndromes.

Authors:  A G Karseras; K M Laurence
Journal:  Br J Ophthalmol       Date:  1975-09       Impact factor: 4.638

7.  Chromosomal abnormalities associated with cyclopia and synophthalmia.

Authors:  R O Howard
Journal:  Trans Am Ophthalmol Soc       Date:  1977
  7 in total

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