(Q36045178)

11 August 2017

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title

Neonatal screening by DNA microarray: spots and chips (English)

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11 August 2017

Nancy S Green

1

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author name string

Kenneth A Pass

series ordinal

2

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11 August 2017

publication date

1 February 2005

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11 August 2017

published in

Nature Reviews Genetics

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11 August 2017

volume

6

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11 August 2017

issue

2

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11 August 2017

page(s)

147-151

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High density synthetic oligonucleotide arrays

11 August 2017

cites work

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DNA chip technology ante portas

21 January 2018

1 reference

Translating cancer genomics into clinical oncology.

21 January 2018

1 reference

Population screening in the age of genomic medicine

21 January 2018

1 reference

Recent developments and new applications of tandem mass spectrometry in newborn screening

21 January 2018

1 reference

Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections

21 January 2018

1 reference

Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for management

21 January 2018

1 reference

Implementation of newborn screening for cystic fibrosis varies widely between states.

21 January 2018

1 reference

Mutational analysis using oligonucleotide microarrays

21 January 2018

1 reference

Genotyping of 22 human papillomavirus types by DNA chip in Korean women: comparison with cytologic diagnosis.

21 January 2018

1 reference

ANX7, a candidate tumor suppressor gene for prostate cancer

21 January 2018

1 reference

The molecular biology of galactosemia

21 January 2018

1 reference

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

21 January 2018

1 reference

Minimizing false-positives in universal newborn hearing screening: a simple solution.

21 January 2018

1 reference

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review

21 January 2018

1 reference

Newborn screening for fragile X syndrome

21 January 2018

1 reference

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

21 January 2018

1 reference

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations

21 January 2018

1 reference

Ethical issues raised by genetic testing with oligonucleotide microarrays

21 January 2018

1 reference

Ethical, legal, and social implications of genomic medicine

21 January 2018

1 reference

DNA diagnosis confirms hemoglobin deletion in newborn screen follow-up

21 January 2018

1 reference

Allelic imbalances in human bladder cancer: genome-wide detection with high-density single-nucleotide polymorphism arrays

31 March 2020

1 reference

A Novel Gene for Neonatal Diabetes Maps to Chromosome 10p12.1-p13

31 March 2020

1 reference

Cystic fibrosis newborn screening: impact on reproductive behavior and implications for genetic counseling

31 March 2020

1 reference

Gene interactions and stroke risk in children with sickle cell anemia

31 March 2020

1 reference

A simple method of screening for the common connexin-26 gene 35delG mutation in nonsyndromic neurosensory autosomal recessive deafness

31 March 2020

1 reference

Newborn hearing screening: will children with hearing loss caused by congenital cytomegalovirus infection be missed?

31 March 2020

1 reference

Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review

31 March 2020

1 reference

Molecular correlations in phenylketonuria: mutation patterns and corresponding biochemical and clinical phenotypes in a heterogeneous California population

31 March 2020

1 reference

Population genetic screening programmes: technical, social and ethical issues

31 March 2020

1 reference

Genetic screening with the DNA chip: a new Pandora's box?

31 March 2020

1 reference

Population-wide infant screening for HLA-based type 1 diabetes risk via dried blood spots from the public health infrastructure

31 March 2020

1 reference

High frequency of leukemic clones in newborn screening blood samples of children with B-precursor acute lymphoblastic leukemia

31 March 2020

1 reference

Data storage and DNA banking for biomedical research: technical, social and ethical issues

31 March 2020

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NRG1526

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Dimensions Publication ID

11 August 2017

1033590111

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