Literature DB >> 1340224

Hemophilia and the use of genetic counseling and carrier testing within family networks.

I Varekamp1, T Suurmeijer, A Bröcker-Vriends, F R Rosendaal.   

Abstract

Entities:  

Mesh：

Year:  1992        PMID： 1340224

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  5 in total

1.  Facilitating family communication about predictive genetic testing: probands' perceptions.

Authors:  Clara L Gaff; Veronica Collins; Tiffany Symes; Jane Halliday
Journal:  J Genet Couns       Date:  2005-04       Impact factor: 2.537

2.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

Authors:  Pascal Borry; Gerry Evers-Kiebooms; Martina C Cornel; Angus Clarke; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

3.  Uptake of Genetic Counseling, Knowledge of Bleeding risks and Psychosocial Impact in a South African Cohort of Female Relatives of People with Hemophilia.

Authors:  Anne Gillham; Brenda Greyling; Tina-Marie Wessels; Bongi Mbele; Rosemarie Schwyzer; Amanda Krause; Johnny Mahlangu
Journal:  J Genet Couns       Date:  2015-04-02       Impact factor: 2.537

4.  DNA testing for fragile X syndrome: implications for parents and family.

Authors:  M A van Rijn; B B de Vries; A Tibben; A M van den Ouweland; D J Halley; M F Niermeijer
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

5.  A family genetic risk communication framework: guiding tool development in genetics health services.

Authors:  Miriam E Wiens; Brenda J Wilson; Christina Honeywell; Holly Etchegary
Journal:  J Community Genet       Date:  2013-01-15
  5 in total

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