(Q38271450)

1 September 2017

1 reference

title

Mosaicism and clinical genetics (English)

1 reference

1 September 2017

Nancy B Spinner

1

1 reference

PubMed ID

25424979

1 September 2017

Laura K Conlin

series ordinal

2

1 reference

1 September 2017

25 November 2014

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American Journal of Medical Genetics Part C: Seminars in Medical Genetics

1 September 2017

1 reference

1 September 2017

166C

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1 September 2017

4

1 reference

1 September 2017

397-405

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Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro.

1 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Chimerism in monochorionic dizygotic twins: case study and review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Detectable clonal mosaicism and its relationship to aging and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Somatic mutations in cerebral cortical malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Confined placental mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Detectable clonal mosaicism from birth to old age and its relationship to cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

A mosaic activating mutation in AKT1 associated with the Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Detectable clonal mosaicism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Conception to ongoing pregnancy: the 'black box' of early pregnancy loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Chimera and other fertilization errors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

THE CHROMOSOME NUMBER OF MAN

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Chromosome instability is common in human cleavage-stage embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31421

21 January 2018

Identifiers

DOI

10.1002/AJMG.C.31421

1 reference

1 September 2017

1 reference

PubMed ID

25424979