K L Greenhalgh

Thrombocytopenia-absent radius syndrome: a clinical genetic study

K L Greenhalgh · Journal of Medical Genetics · 2002 · 190 citations · Full text

Life Sciences, Cardiology, Genetics +17

22q11 deletion: a multisystem disorder requiring multidisciplinary input

K L Greenhalgh · Archives of Disease in Childhood · 2003 · 29 citations · Full text

Life Sciences, Genetics, Pediatrics +17

Muir-Torre Syndrome: expanding the genotype and phenotype—a further family with a MSH6 mutation

Helen Murphy, Robert W. Armstrong, Diane Cairns et al. · Familial Cancer · 2008 · 24 citations

Life Sciences, Genetics, Molecular Genetics +10

Hypoglycaemic syncope in children secondary to beta-blockers

Tarique Hussain, K L Greenhalgh, Karen McLeod · Archives of Disease in Childhood · 2009 · 16 citations

Medicine, Cardiology, Pediatrics +17

Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants

Lucy Loong, Cankut Çubuk, Subin Choi et al. · Genetics in Medicine · 2021 · 16 citations · Full text

Life Sciences, Bioinformatics, Molecular Genetics +14