Literature DB >> 3781563

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

A Schinzel.   

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Year:  1986        PMID： 3781563     DOI： 10.1007/bf00282561

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


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  6 in total

1.  Recurrence risk in de novo 21q21q translocation Down syndrome.

Authors:  B D Hall
Journal:  Am J Med Genet       Date:  1985-10

2.  Prenatal diagnosis and the Prader-Willi syndrome.

Authors:  A Smith
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

3.  Recurrence risk in 21q/21q translocation of Down syndrome.

Authors:  K L Garver; S G Marchese; M W Steele; D M Ketterer
Journal:  J Pediatr       Date:  1982-02       Impact factor: 4.406

4.  Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.

Authors:  T A Donlon; M Lalande; A Wyman; G Bruns; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

5.  A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors:  A Smith; M Noel
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  Cytogenetic studies of familial Prader-Willi syndrome.

Authors:  T Hasegawa; M Hara; M Ando; M Osawa; Y Fukuyama; M Takahashi; K Yamada
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  6 in total
  2 in total

Review 1.  Microdeletion syndromes, balanced translocations, and gene mapping.

Authors:  A Schinzel
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

2.  A report on seven fetal cases associated with 15q11-q13 microdeletion and microduplication.

Authors:  Xiuzhu Huang; Jieping Chen; Wenlong Hu; Lu Li; Huiyan He; Hui Guo; Qiuyan Liao; Mei Ye; Donge Tang; Yong Dai
Journal:  Mol Genet Genomic Med       Date:  2021-02-04       Impact factor: 2.183
  2 in total

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