(Q33778081)

29 July 2017

Visualization of fine-scale genomic structure by oligonucleotide-based high-resolution FISH. (English)

1 reference

29 July 2017

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N A Yamada

1

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29 July 2017

L S Rector

2

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29 July 2017

P Tsang

3

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29 July 2017

E Carr

4

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29 July 2017

A Scheffer

5

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29 July 2017

M C Sederberg

6

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29 July 2017

M E Aston

7

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29 July 2017

R A Ach

8

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29 July 2017

A Tsalenko

9

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29 July 2017

N Sampas

10

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29 July 2017

B Peter

11

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29 July 2017

L Bruhn

12

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29 July 2017

A R Brothman

13

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29 July 2017

18 December 2010

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Cytogenetics and Genome Research

29 July 2017

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29 July 2017

132

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29 July 2017

248-254

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29 July 2017

4

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Array-based comparative genome hybridization in clinical genetics.

29 July 2017

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NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

21 January 2018

1 reference

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

Joubert syndrome: insights into brain development, cilium biology, and complex disease

21 January 2018

1 reference

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

21 January 2018

1 reference

Molecular cytogenetics: diagnosis and prognostic assessment

21 January 2018

1 reference

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

21 January 2018

1 reference

PROBER: oligonucleotide FISH probe design software.

21 January 2018

1 reference

The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome

21 January 2018

1 reference

Multiplex amplification of large sets of human exons

21 January 2018

1 reference

Advances in fluorescence in situ hybridization

21 January 2018

1 reference

Ultra-sensitive FISH using peroxidase-mediated deposition of biotin- or fluorochrome tyramides.

21 January 2018

1 reference

Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

21 January 2018

1 reference

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

The new cytogenetics: blurring the boundaries with molecular biology

21 January 2018

1 reference

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

21 January 2018

1 reference

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

21 January 2018

1 reference

Guidance for fluorescence in situ hybridization testing in hematologic disorders

21 January 2018

1 reference

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000322717

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29 July 2017

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