1.
The MBRRACE-UK perinatal surveillance report
by Ward Platt, Martin
Archives of disease in childhood. Fetal and neonatal edition, 2016-01, Vol.101 (1), p.4-5

2.
Patterns of child death in England and Wales
by Sidebotham, Peter, Dr
The Lancet (British edition), 2014, Vol.384 (9946), p.904-914

3.
Demand weaning: infants’ answer to professionals’ dilemmas
by Ward Platt, Martin P
Archives of disease in childhood, 2009-02, Vol.94 (2), p.79-80

4.
“New” practice of bedsharing and risk of SIDS
by Ball, Helen L
The Lancet (British edition), 2004-05-08, Vol.363 (9420), p.1558-1558

5.
Weight gain and sudden infant death syndrome: changes in weight z scores may identify infants at increased risk
by Blair, Peter S
Archives of disease in childhood, 2000-06, Vol.82 (6), p.462-469

6.
Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 ( MCT8) Gene
by Schwartz, Charles E
American journal of human genetics, 2005, Vol.77 (1), p.41-53

7.

8.
Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13...
by Cardoso, Carlos
American journal of human genetics, 2003-04, Vol.72 (4), p.918-930

9.
The Choice of Normative Pediatric Reference Database Changes Spine Bone Mineral Density Z-Scores But Not the Relationship Between Bone Mineral Density and Prevalent Vertebral Fract...
by Ma, Jinhui
The journal of clinical endocrinology and metabolism, 2015-03, Vol.100 (3), p.1018-1027

10.
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
by del Gaudio, Daniela
Genetics in medicine, 2006-12, Vol.8 (12), p.784-792

11.
Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan
by Carss, Keren J
American journal of human genetics, 2013-07-11, Vol.93 (1), p.29-41

12.
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients
by Hexter, Adam
Journal of Medical Genetics, 2015-10, Vol.52 (10), p.699-705

13.
Simons Variation in Individuals Project (Simons VIP): A Genetics-First Approach to Studying Autism Spectrum and Related Neurodevelopmental Disorders
by Consortium, The Simons Vip
Neuron (Cambridge, Mass.), 2012-03-22, Vol.73 (6), p.1063-1067

14.
Update on the emergency medical treatment of anaphylactic reactions for first medical responders and for community nurses
by Project Team of The Resuscitation Council (UK)
Emergency medicine journal : EMJ, 2001-09, Vol.18 (5), p.393-395

15.
Sudden infant death syndrome in infants evaluated by apnea programs in California
by DAVIDSON WARD, S. L
Pediatrics (Evanston), 1986, Vol.77 (4), p.451-458
