Introductory Speech for Robert J. Gorlin

Por Hall, Judith G.
Publicado em 2005

Advances in human genetics

Por Hall, Judith G.
Publicado em 1990

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

Por Hall, Judith G.
Publicado em 1981

The genetics and heterogeneity of common gastrointestinal disorders

Por Hall, Judith G.
Publicado em 1982

Genetic disorders—Syndromology and prenatal diagnosis

Por Hall, Judith G.
Publicado em 1983

Congenital malformations: Case studies in developmental anatomy

Por Hall, Judith G.
Publicado em 1974

Malformation syndromes

Por Hall, Judith G.
Publicado em 1975

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

Por Hall, Judith G.
Publicado em 2003

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

Por Hall, Judith G
Publicado em 2004

Paediatrician Resource Survey: Preliminary results suggest some urgency

Por Hall, Judith G
Publicado em 2001

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

Por Hall, Judith G
Publicado em 2011

Epigenetics: What does it mean for paediatric practice?

Por Hall, Judith G
Publicado em 2014

Reflections on an academic career

Por Hall, Judith G.
Publicado no Mol Genet Genomic Med (2017)

Be prepared for prenatal diagnosis

Por Hall, Judith G
Publicado no Eur J Hum Genet (2017)

Using the Term Amyoplasia Loosely Can Lead to Confusion

Por Hall, Judith G.
Publicado no Am J Hum Genet (2020)

Arthrogryposis as a Syndrome: Gene Ontology Analysis

Por Hall, Judith G., Kiefer, Jeff
Publicado no Mol Syndromol (2016)

INHERITED DISORDERS OF THE SKELETON

Por Reed, Susan D., Hall, Judith G.
Publicado em 1980

Tuberous sclerosis: case report and investigation of family members

Por Wilson, R. Douglas, Hall, Judith G., McGillivray, Barbara C.
Publicado em 1985

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

Por 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
Publicado em 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...

Por 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
Publicado em 2013