Introductory Speech for Robert J. Gorlin

door Hall, Judith G.
Gepubliceerd in 2005

Advances in human genetics

door Hall, Judith G.
Gepubliceerd in 1990

March of dimes annual review of birth defects, 1978. Part B. Penetrance and variability in malformation syndromes

door Hall, Judith G.
Gepubliceerd in 1981

The genetics and heterogeneity of common gastrointestinal disorders

door Hall, Judith G.
Gepubliceerd in 1982

Genetic disorders—Syndromology and prenatal diagnosis

door Hall, Judith G.
Gepubliceerd in 1983

Congenital malformations: Case studies in developmental anatomy

door Hall, Judith G.
Gepubliceerd in 1974

Malformation syndromes

door Hall, Judith G.
Gepubliceerd in 1975

Individualized medicine. What the genetic revolution will bring to health care in the 21st century.

door Hall, Judith G.
Gepubliceerd in 2003

How is the progress in genetics relevant to children’s health care

door Hall, Judith G
Gepubliceerd in 2004

Paediatrician Resource Survey: Preliminary results suggest some urgency

door Hall, Judith G
Gepubliceerd in 2001

Over the years, I hope I’ve learned a few things to pass along!

door Hall, Judith G
Gepubliceerd in 2011

Epigenetics: What does it mean for paediatric practice?

door Hall, Judith G
Gepubliceerd in 2014

Reflections on an academic career

door Hall, Judith G.
Gepubliceerd in Mol Genet Genomic Med (2017)

Be prepared for prenatal diagnosis

door Hall, Judith G
Gepubliceerd in Eur J Hum Genet (2017)

Using the Term Amyoplasia Loosely Can Lead to Confusion

door Hall, Judith G.
Gepubliceerd in Am J Hum Genet (2020)

Arthrogryposis as a Syndrome: Gene Ontology Analysis

door Hall, Judith G., Kiefer, Jeff
Gepubliceerd in Mol Syndromol (2016)

INHERITED DISORDERS OF THE SKELETON

door Reed, Susan D., Hall, Judith G.
Gepubliceerd in 1980

Tuberous sclerosis: case report and investigation of family members

door Wilson, R. Douglas, Hall, Judith G., McGillivray, Barbara C.
Gepubliceerd in 1985

A meeting of minds: interdisciplinary research in the health sciences in Canada

door Hall, Judith G., Bainbridge, Lesley, Buchan, Alison, Cribb, Alastair, Drummond, Jane, Gyles, Carlton, Hicks, T. Philip, McWilliam, Carol, Paterson, Barbara, Ratner, Pamela A., Skarakis-Doyle, Elizabeth, Solomon, Patty
Gepubliceerd in 2006

A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with marfan and loeys–dietz syndrome...

door Rienhoff, Hugh Young, Yeo, Chang-Yeol, Morissette, Rachel, Khrebtukova, Irina, Melnick, Jonathan, Luo, Shujun, Leng, Nan, Kim, Yeon-Jin, Schroth, Gary, Westwick, John, Vogel, Hannes, McDonnell, Nazli, Hall, Judith G, Whitman, Malcolm
Gepubliceerd in 2013