Suchergebnisse - "Marshall, Mhairi S"

PubPharm (10)

1

Germline ERBB3 mutation in familial non-small cell lung carcinoma: expanding ErbB’s role in oncogenesis

enthalten in: bioRxiv.org | 2021

von McInerney-Leo, A. | Chew, H. | Inglis, P. | +17

2

Germline ERBB3 mutation in familial non-small-cell lung carcinoma : expanding ErbB's role in oncogenesis

enthalten in: Human molecular genetics | 2021

von McInerney-Leo, A. | Chew, H. | Inglis, P. | +17

3

HLA Alleles Associated With Risk of Ankylosing Spondylitis and Rheumatoid Arthritis Influence the Gut Microbiome

enthalten in: Arthritis & rheumatology (Hoboken, N.J.) | 2019

von Asquith, M. | Sternes, P. | Costello, M. | +9

4

HLA Alleles Associated With Risk of Ankylosing Spondylitis and Rheumatoid Arthritis Influence the Gut Microbiome

enthalten in: Arthritis & Rheumatology | 2019

von Asquith, M. | Sternes, P. | Costello, M. | +9

5

Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement : Extending the phenotypic spectrum

enthalten in: American journal of medical genetics. Part A | 2017

von McInerney-Leo, A. | Wheeler, L. | Marshall, M. | +6

6

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects

enthalten in: Human molecular genetics | 2015

von McInerney-Leo, A. | Sparrow, D. | Harris, J. | +9

7

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects

enthalten in: Human molecular genetics | 2015

von McInerney-Leo, A. | Sparrow, D. | Harris, J. | +9

8

Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas

enthalten in: Clinical endocrinology | 2014

von McInerney-Leo, A. | Marshall, M. | Gardiner, B. | +7

CommentIn: Clin Endocrinol (Oxf). 2014 Jan;80(1):23-4. - PMID 24168015

9

Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas

enthalten in: Clinical endocrinology | 2014

von McInerney‐Leo, A. | Marshall, M. | Gardiner, B. | +7

10

Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome

enthalten in: BoneKEy reports | 2013

von McInerney-Leo, A. | Marshall, M. | Gardiner, B. | +12

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