Literature DB >> 7327577

Ring chromosome 16.

L Neidengard, R S Sparkes.   

Abstract

Mesh：

Year:  1981        PMID： 7327577     DOI： 10.1007/bf00293072

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  6 in total

1.  Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions.

Authors:  J Boué; P Lazar
Journal:  Teratology       Date:  1975-08

2.  Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21).

Authors:  J P Fryns; S Melchoir; J Jaeken; H van den Berghe
Journal:  Hum Genet       Date:  1977-10-14       Impact factor: 4.132

3.  Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.

Authors:  S H Roberts; D P Duckett
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

4.  Five familial cases with a trisomy 16p syndrome due to translocation.

Authors:  N J Leschot; J J De Nef; J P Geraedts; M J Becker-Bloemkolk; A Talma; J B Bijlsma; M Verjaal
Journal:  Clin Genet       Date:  1979-09       Impact factor: 4.438

5.  Trisomy 16q arising from a maternal 15p;16q translocation.

Authors:  M A Ridler; J A McKeown
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

6.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438
  6 in total
  4 in total

1.  Identical twins with deletion 16q syndrome: evidence that 16q12.2-q13 is the critical band region.

Authors:  F F Elder; J W Ferguson; L H Lockhart
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

Authors:  D F Callen; H Eyre; S Lane; Y Shen; I Hansmann; N Spinner; E Zackai; D McDonald-McGinn; S Schuffenhauer; J Wauters
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

3.  Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Authors:  A O Wilkie; V J Buckle; P C Harris; J Lamb; N J Barton; S T Reeders; R H Lindenbaum; R D Nicholls; M Barrow; N C Bethlenfalvay
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

4.  Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic Hybridization.

Authors:  Pietro Cignini; Angela Dinatale; Laura D'Emidio; Annamaria Giacobbe; Elisa Maria Pappalardo; Santina Ermito; Domenico Bizzoco; Gianluca Di Giacomo; Ivan Gabrielli; Alvaro Mesoraca; Maurizio Giorlandino; Claudio Giorlandino
Journal:  AJP Rep       Date:  2011-03-18
  4 in total

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