Introductory Speech for Robert J. Gorlin

Tekijä Hall, Judith G.
Julkaistu 2005

Advances in human genetics

Tekijä Hall, Judith G.
Julkaistu 1990

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

Tekijä Hall, Judith G.
Julkaistu 1981

The genetics and heterogeneity of common gastrointestinal disorders

Tekijä Hall, Judith G.
Julkaistu 1982

Genetic disorders—Syndromology and prenatal diagnosis

Tekijä Hall, Judith G.
Julkaistu 1983

Congenital malformations: Case studies in developmental anatomy

Tekijä Hall, Judith G.
Julkaistu 1974

Malformation syndromes

Tekijä Hall, Judith G.
Julkaistu 1975

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

Tekijä Hall, Judith G.
Julkaistu 2003

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

Tekijä Hall, Judith G
Julkaistu 2004

Paediatrician Resource Survey: Preliminary results suggest some urgency

Tekijä Hall, Judith G
Julkaistu 2001

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

Tekijä Hall, Judith G
Julkaistu 2011

Epigenetics: What does it mean for paediatric practice?

Tekijä Hall, Judith G
Julkaistu 2014

Reflections on an academic career

Tekijä Hall, Judith G.
Julkaisussa Mol Genet Genomic Med (2017)

Be prepared for prenatal diagnosis

Tekijä Hall, Judith G
Julkaisussa Eur J Hum Genet (2017)

Using the Term Amyoplasia Loosely Can Lead to Confusion

Tekijä Hall, Judith G.
Julkaisussa Am J Hum Genet (2020)

Arthrogryposis as a Syndrome: Gene Ontology Analysis

Tekijä Hall, Judith G., Kiefer, Jeff
Julkaisussa Mol Syndromol (2016)

INHERITED DISORDERS OF THE SKELETON

Tekijä Reed, Susan D., Hall, Judith G.
Julkaistu 1980

Tuberous sclerosis: case report and investigation of family members

Tekijä Wilson, R. Douglas, Hall, Judith G., McGillivray, Barbara C.
Julkaistu 1985

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

Tekijä 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
Julkaistu 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...

Tekijä 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
Julkaistu 2013