author-photo

M Ireland

Newcastle University

13

Papers

556

Citations

Citation Trend

Filter By

Papers (9) Sort By

Journal Conference Others

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3

2004 Human Genetics
Show All
- Source
- Cite
- Save
Citations (42)
Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes

1999 Human Genetics
Show All
- Source
- Cite
- Save
Citations (21)
Behavioural phenotype of Cornelia de Lange syndrome

1999 Archives of Disease in Childhood
Show All
- Source
- Cite
- Save
Citations (128)
Second‐trimester pregnancy associated plasma protein‐A levels are reduced in Cornelia de Lange syndrome pregnancies

1999 Prenatal Diagnosis
Show All
- Source
- Cite
- Save
Citations (50)
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

1997 Journal of Medical Genetics
Show All
- Source
- Cite
- Save
Citations (59)
Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.

1995 Journal of Medical Genetics
Show All
- Source
- Cite
- Save
Citations (28)
Mapping of Simpson – Golabi – Behmel syndrome to Xq25 – q27

1994 Human Molecular Genetics
Show All
- Source
- Cite
- Save
Citations (40)
Brachmann-de Lange syndrome. Delineation of the clinical phenotype

1993 American Journal of Medical Genetics
Show All
- Source
- Cite
- Save
Citations (99)
A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.

1991 Journal of Medical Genetics
Show All
- Source
- Cite
- Save
Citations (55)