Literature DB >> 3957352

Prenatal diagnosis and the Prader-Willi syndrome.

A Smith.   

Abstract

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Year:  1986        PMID： 3957352     DOI： 10.1007/bf00291897

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


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  4 in total

Review 1.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation.

Authors:  N Niikawa; S Ishikiriyama
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Parental origin of chromosome 15 deletion in Prader-Willi syndrome.

Authors:  M G Butler; C G Palmer
Journal:  Lancet       Date:  1983-06-04       Impact factor: 79.321

4.  Chromosome 15 in Prader-Willi syndrome.

Authors:  C N Fear; D E Mutton; A C Berry; J Z Heckmatt; V Dubowitz
Journal:  Dev Med Child Neurol       Date:  1985-06       Impact factor: 5.449
  4 in total
  2 in total

1.  Prader-willi syndrome: A case report and a Chinese literature review.

Authors:  Junzhen Zhu; Qinying Cao; Ning Zhang; Lijuan Zhao
Journal:  Intractable Rare Dis Res       Date:  2013-11

2.  Approaches to the prenatal diagnosis of the Prader-Willi syndrome.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132
  2 in total

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