(Q41252923)

28 September 2017

1 reference

title

Pitfalls in the interpretation of molecular diagnostic tests (English)

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28 September 2017

Korf BR

1

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28 September 2017

language of work or name

1 reference

1 January 1996

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Journal of Clinical Laboratory Analysis

28 September 2017

published in

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28 September 2017

volume

10

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28 September 2017

issue

6

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28 September 2017

page(s)

368-374

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The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing

28 September 2017

cites work

1 reference

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Antenatal screening for carriers of cystic fibrosis: randomised trial of stepwise v couple screening

21 January 2018

1 reference

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Tay-Sachs disease--carrier screening, prenatal diagnosis, and the molecular era. An international perspective, 1970 to 1993. The International TSD Data Collection Network

21 January 2018

1 reference

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Universal community carrier screening for cystic fibrosis?

21 January 2018

1 reference

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

1 reference

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DNA diagnosis for the detection of sickle hemoglobinopathies

21 January 2018

1 reference

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Screening for carriers of Tay-Sachs disease among Ashkenazi Jews. A comparison of DNA-based and enzyme-based tests

21 January 2018

1 reference

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21 January 2018

Molecular diagnosis (2)

1 reference

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The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

21 January 2018

1 reference

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Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2825%281996%2910%3A6%3C368%3A%3AAID-JCLA8%3E3.0.CO%3B2-2

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

21 January 2018

1 reference

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Non-paternity and prenatal genetic screening

21 January 2018

1 reference

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Efficient 12-mutation testing in the CFTR gene: a general model for complex mutation analysis

21 January 2018

1 reference

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Correlation between genotype and phenotype in patients with cystic fibrosis

21 January 2018

1 reference

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The molecular genetics of tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2825%281996%2910%3A6%3C368%3A%3AAID-JCLA8%3E3.0.CO%3B2-2

Prevalence of cystic fibrosis in fetuses with dilated bowel

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2825%281996%2910%3A6%3C368%3A%3AAID-JCLA8%3E3.0.CO%3B2-2

10.1002/(SICI)1098-2825(1996)10:6<368::AID-JCLA8>3.0.CO;2-2

21 January 2018

Identifiers

DOI

1 reference

28 September 2017

1 reference