Literature DB >> 11807908

Parents of children with spinal muscular atrophy are not obligate carriers: carrier testing is important for reproductive decision-making.

Susan Zeesman, Donald T Whelan, Nancy Carson, Jean McGowan-Jordan, Tracy L Stockley, Peter N Ray, Thomas W Prior.   

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Year:  2002        PMID： 11807908     DOI： 10.1002/ajmg.10132

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases.

Authors:  Mahmoud Shekari Khaniani; Sima Mansoori Derakhshan; Shamsei Abasalizadeh
Journal:  J Prenat Med       Date:  2013-07

2.  Single-sperm analysis for recurrence risk assessment of spinal muscular atrophy.

Authors:  Philippe Burlet; Nadine Gigarel; Maryse Magen; Séverine Drunat; Alexandra Benachi; Laetitia Hesters; Arnold Munnich; Jean-Paul Bonnefont; Julie Steffann
Journal:  Eur J Hum Genet       Date:  2009-11-11       Impact factor: 4.246

3.  SMN1 dosage analysis in spinal muscular atrophy from India.

Authors:  Akanchha Kesari; Hanna Rennert; Debra G B Leonard; Balraj Mittal
Journal:  BMC Med Genet       Date:  2005-05-23       Impact factor: 2.103

4.  D5S351 and D5S1414 located at the spinal muscular atrophy critical region represent novel informative markers in the Iranian population.

Authors:  Maryam Sedghi; Sadeq Vallian
Journal:  Meta Gene       Date:  2015-11-10
  4 in total

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