Literature DB >> 5314801

A single nasal orifice and severe intrauterine growth retardation in a case of 46, XX, 18 r.

R L Neu, N Watanabe, L I Gardner, A G Galvis.   

Abstract

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Year:  1971        PMID： 5314801

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  6 in total

1.  Further studies on the genetic heterogeneity of cebocephaly.

Authors:  G I Lazjuk; I W Lurie; M K Nedzved
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

4.  Genetic heterogeneity of cebocephaly.

Authors:  L B Holmes; S Driscoll; L Atkins
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

5.  Adults with Chromosome 18 Abnormalities.

Authors:  Bridgette Soileau; Minire Hasi; Courtney Sebold; Annice Hill; Louise O'Donnell; Daniel E Hale; Jannine D Cody
Journal:  J Genet Couns       Date:  2014-11-19       Impact factor: 2.537

6.  Descriptive neuropathology of chromosomal disorders in man.

Authors:  F Gullotta; H Rehder; A Gropp
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  6 in total

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