Literature DB >> 9240752

Trisomy 17 detected in amniotic fluid cells but not in newborn infant.

M G Butler, R L Neu, K Mitchell.   

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Year:  1996        PMID： 9240752      PMCID： PMC5977976          DOI： 10.1002/ajmg.1320650402

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


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  4 in total

1.  A second-generation linkage map of the human genome.

Authors:  J Weissenbach; G Gyapay; C Dib; A Vignal; J Morissette; P Millasseau; G Vaysseix; M Lathrop
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

2.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

3.  Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

Authors:  A Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; A Chakravarti; D H Ledbetter
Journal:  Hum Mol Genet       Date:  1993-02       Impact factor: 6.150

4.  Mosaic trisomy 17 in amniotic fluid cells not confirmed in the newborn.

Authors:  M Djalali; G Barbi; D Grab
Journal:  Prenat Diagn       Date:  1991-06       Impact factor: 3.050
  4 in total
  2 in total

1.  Trisomy 17 mosaicism in a four-year seven-month-old white girl: follow-up report.

Authors:  M G Butler
Journal:  Prenat Diagn       Date:  1999-07       Impact factor: 3.050

2.  Mosaic trisomy 17: variable clinical and cytogenetic presentation.

Authors:  Robert Daber; Kimberly A Chapman; Eduardo Ruchelli; Stefanie Kasperski; Surabhi Mulchandani; Brian D Thiel; Hakon Hakonarson; Elaine H Zackai; Laura K Conlin; Nancy B Spinner
Journal:  Am J Med Genet A       Date:  2011-10       Impact factor: 2.802
  2 in total

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