J. McKie

发表

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

J. Osinga, R. Hofstra, B. Dallapiccola, 1999, American journal of human genetics.

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

R. Kucherlapati, S. Weissman, R. Shprintzen, 1997, American journal of human genetics.

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

P. Scambler, A. Baldini, S. Halford, 1996, American journal of human genetics.

Adverse childhood experiences, epigenetics and telomere length variation in childhood and beyond: a systematic review of the literature

C. Gillberg, H. Minnis, Jason Lang, 2019, European Child & Adolescent Psychiatry.

A human gene similar to Drosophila melanogaster peanut maps to the DiGeorge syndrome region of 22q11

P. Scambler, U. Kim, H. Sutherland, 1997, Human Genetics.

Direct selection of conserved cDNAs from the DiGeorge critical region: isolation of a novel CDC45-like gene.

P. Scambler, H. Sutherland, R. Wadey, 1998, Genome research.

The Nfe2l1 gene maps to distal mouse Chromosome 11

P. Scambler, J. McKie, 2009, Mammalian Genome.

Cloning and mapping of murine Nfe2l1.

P. Scambler, M. Mattei, K. Johnstone, 1995, Genomics.

Hira, a gene from the DGS/VCFS region, is required for normal embryogenesis.

Lui, Peter J. Scambler, Catherine Roberts, 1998 .

Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome

K. Hirschhorn, B. Levy, C. Bancroft, 2000, Mammalian Genome.