C. Greenberg

D. Jassal, V. Ariyarajah, C. Greenberg, 2008, Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance.

Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population

C. Ober, K. Boycott, A. Innes, 2016, Molecular genetics & genomic medicine.

Development of a Population-Based Newborn Screening Method for Severe Combined Immunodeficiency in Manitoba, Canada

P. V. Van Caeseele, J. Thompson, C. Greenberg, 2018, International journal of neonatal screening.

Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.

J. Graham, E. Friedberg, L. Meira, 2000, American journal of human genetics.

Congenital rickets caused by maternal vitamin D deficiency.

C. Greenberg, A. Chudley, C. Prasad, 2002, Paediatrics & child health.

Replacement of arginine 773 by cysteine or histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes.

D. Belsham, Chawnshang Chang, J. Trapman, 1992, American journal of human genetics.

Hypophosphatasia: Canadian update on diagnosis and management

S. Van Uum, C. Greenberg, R. Josse, 2019, Osteoporosis International.

DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.

J. Hamerton, C. Greenberg, K. Wrogemann, 1987, American journal of human genetics.

Clinical genetics and the Hutterite population: A review of Mendelian disorders

K. Boycott, F. Bernier, A. Innes, 2008, American journal of medical genetics. Part A.

Amerindian pyruvate carboxylase deficiency is associated with two distinct missense mutations.

M. A. Carbone, D. Cole, C. Greenberg, 1998, American journal of human genetics.

A new autosomal recessive lethal chondrodystrophy with congenital hydrops.

D. Rimoin, H. Gruber, C. Greenberg, 1988, American journal of medical genetics.

Lattice corneal dystrophy type I

D. Kwiatkowski, C. Greenberg, C. Maury, 2020, Definitions.

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.

J. Hamerton, C. Greenberg, A. Chudley, 1990, American journal of medical genetics.

Tracheal agenesis and associated malformations: a comparison with tracheoesophageal fistula and the VACTERL association.

C. Greenberg, J. Evans, J. Reggin, 1985, American journal of medical genetics.

A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred

C. Greenberg, B. Bapat, G. Charames, 2008, Human Genetics.

Newborn Screening by Tandem Mass Spectrometry

B. Potter, C. Greenberg, D. Avard, 2007, Canadian journal of public health = Revue canadienne de sante publique.

Increased plasma pyridoxal-5′-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia

C. Greenberg, S. Coburn, B. Chodirker, 1990, Journal of Inherited Metabolic Disease.

Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort.

C. Greenberg, O. Mamer, D. Lambert, 1999, Molecular genetics and metabolism.

Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome.

C. Stanley, B. Y. Hsu, C. Greenberg, 2001, The Journal of pediatrics.

Variability in the storage and use of newborn dried bloodspots in Canada: is it time for national standards?

C. Laberge, C. Greenberg, D. Avard, 2006, Genomics, society, and policy.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

C. Greenberg, T. Weiler, K. Morgan, 1998, American journal of human genetics.

Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction.

C. Greenberg, K. Wrogemann, W. Halliday, 1991, American journal of medical genetics.

GENE STUDIES IN NEWBORN MALES WITH DUCHENNE MUSCULAR DYSTROPHY DETECTED BY NEONATAL SCREENING

C. Greenberg, K. Wrogemann, E. Nylen, 1988, The Lancet.

Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds.

C. Greenberg, A. Chudley, B. McClarty, 1991, The Journal of pediatrics.

Comparison of the Segregation of the RYR1 C1840T Mutation with Segregation of the Caffeine/Halothane Contracture Test Results for Malignant Hyperthermia Susceptibility in a Large Manitoba Mennonite Family

M. Phillips, D. Bose, C. Greenberg, 1996, Anesthesiology.

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

J. Beckmann, K. Bushby, H. Goebel, 2000, Neuromuscular Disorders.

inactivation (see comments) unrelated males based on studies of maternal T cell X chromosome Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two

K. Siminovitch, J. Puck, M. Poncz, 2011 .

Manitoba oculotrichoanal (MOTA) syndrome: Report of eight new cases

J. M. van de Kamp, A. Slavotinek, C. Greenberg, 2007, American journal of medical genetics. Part A.

Reflex Seizures in a Patient with CDKL5 Deficiency Disorder

J. Appendino, J. N. Hartley, C. Greenberg, 2019, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Emergency treatment in glutaryl-CoA dehydrogenase deficiency

C. Greenberg, S. Kölker, G. Hoffmann, 2004, Journal of Inherited Metabolic Disease.

Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship.

C. Greenberg, T. Perry, W. Rhead, 1989, The Journal of pediatrics.

Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite community.

J. Girard, C. Greenberg, P. Kamoun, 2001, Molecular genetics and metabolism.

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

L. Kunkel, A. Covone, N. Archidiacono, 1989, American journal of human genetics.

Infantile hypophosphatasia--linkage with the RH locus.

C. Greenberg, J. Evans, B. Chodirker, 1987, Genomics.

Outcome of perinatal hypophosphatasia in manitoba mennonites: a retrospective cohort analysis.

C. Greenberg, M. Whyte, E. Leung, 2013, JIMD reports.

Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

Johannes Zschocke, Thomas Opladen, I. Harting, 2017, Journal of Inherited Metabolic Disease.

Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism

C. Greenberg, C. Prasad, B. Chodirker, 2007, Congenital anomalies.

Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.

J. Thompson, C. Greenberg, C. Prasad, 2001, Molecular genetics and metabolism.

New horizons in neonatal screening - Lessons from a pilot. Neonatal screening programme for duchenne muscular dystrophy

C. Greenberg, H. Jacobs, 1995 .

DNA analysis for detection of medium-chain acyl-CoA dehydrogenase deficiency in a Manitoba newborn population

J. Thompson, C. Greenberg, C. Gregory, 1995 .

A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type I.

C. Greenberg, A. Chudley, S. Goodman, 1995, Human molecular genetics.

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project

Gary L Hoffman, Alicia Roberts, Stephen M Downs, 2011, Genetics in Medicine.

Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade of experience.

C. Greenberg, A. Schlune, S. Kölker, 2012, Molecular genetics and metabolism.

Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models—a cohort study in 180 patients

A. Ribes, C. Greenberg, S. Kölker, 2014, Journal of Inherited Metabolic Disease.

Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort.

M. D. Del Bigio, C. Greenberg, S. Kölker, 2005, Brain : a journal of neurology.

Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

J. Thompson, C. Greenberg, C. Prasad, 2002, Molecular genetics and metabolism.

Atypical presentation of Wiskott-Aldrich syndrome: diagnosis in two unrelated males based on studies of maternal T cell X chromosome inactivation.

K. Siminovitch, J. Puck, M. Poncz, 1990, Blood.

Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.

P. Choyke, W. Linehan, L. Schmidt, 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

ENT abnormalities associated with Fraser syndrome: case report and literature review.

C. Greenberg, B. Levin, M. M. Mina, 1988, The Journal of otolaryngology.

Mucopolysaccharidosis I presenting with endocardial fibroelastosis of infancy.

C. Greenberg, R. Wenstrup, C. Greenberg, 1989, American journal of diseases of children.

Enzyme-replacement therapy in life-threatening hypophosphatasia.

Nick Bishop, José Luis Millán, Matthew Downs, 2012, The New England journal of medicine.

A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites.

C. Greenberg, B. Chodirker, C. L. Taylor, 1993, Genomics.

The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations

K. Bushby, M. Zatz, C. Greenberg, 2005, Human mutation.

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).

C. Greenberg, T. Weiler, R. Bashir, 1999, Human molecular genetics.

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.

C. Stanley, B. Y. Hsu, M. Poncz, 1998, The New England journal of medicine.

Evolutionary Comparison Provides Evidence for Pathogenicity of RMRP Mutations

A. Reymond, E. Dermitzakis, C. Ucla, 2005, PLoS genetics.

Molecular characterization of the marker chromosome associated with cat eye syndrome.

B. Emanuel, M. Budarf, H. McDermid, 1994, American journal of human genetics.

Agenesis of the penis: patterns of associated malformations.

C. Greenberg, A. Chudley, J. Evans, 1999, American journal of medical genetics.

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.

Lei Zhou, B. Gelb, D. Chitayat, 1999, Human molecular genetics.

Identification of an uncommon haptoglobin type using DNA and protein analysis

N. Maeda, C. Greenberg, S. Marles, 1993, Human Genetics.

Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons.

D. Yan, J. Hamerton, C. Greenberg, 1992, American journal of medical genetics.

review of genetic screening criteria gastric cancer: assessment of 42 new families and Germline E-cadherin mutations in hereditary diffuse

W. Foulkes, J. Senz, C. Greenberg, 2006 .

Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria

W. Foulkes, Y. Butterfield, C. Caldas, 2004, Journal of Medical Genetics.

Reproductive fitness in maternal homocystinuria due to cystathionine β-synthase deficiency

S. Rosengren, E. Roeder, S. Waisbren, 2002, Journal of Inherited Metabolic Disease.

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

W. Linehan, L. Schmidt, B. Zbar, 2001, American journal of human genetics.

Tracheal agenesis revisited: analysis of associated anomalies.

C. Greenberg, J. Evans, L. Erdile, 1999, American journal of medical genetics.

Predictive, pre‐natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000

B. Fernandez, M. Hayden, W. Meschino, 2003, Clinical genetics.

Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.

M. Hayden, O. Suchowersky, J. Theilmann, 1992, American journal of medical genetics.

Hypophosphatasia: Enzyme Replacement Therapy (Asfotase Alfa) Decreases TNSALP Substrate Accumulation And Improves Functional Outcomes In Affected Adolescents And Adults.

H. Plotkin, C. Greenberg, M. Whyte, 2012 .

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

C. Greenberg, T. Weiler, K. Morgan, 1996, American journal of human genetics.

Quantitative Acylcarnitine Profiling in Peripheral Blood Mononuclear Cells Using In Vitro Loading With Palmitic and 2-Oxoadipic Acids: Biochemical Confirmation of Fatty Acid Oxidation and Organic Acid Disorders

H. Schulze‐Bergkamen, E. Mayatepek, C. Greenberg, 2005, Pediatric Research.

A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort

G. Hatch, A. Elliott, L. Simard, 2013, Journal of Medical Genetics.

Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.

C. Greenberg, A. Chudley, S. Marles, 1995, American journal of medical genetics.

Increased occurrence of cleft lip in glycogen storage disease type II (GSDII): exclusion of a contiguous gene syndrome in two patients by presence of intragenic mutations including a novel nonsense mutation Gln58Stop.

P. Arn, C. Greenberg, R. Hirschhorn, 1999, American journal of medical genetics.

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene.

C. Greenberg, T. Weiler, P. Frosk, 2002, American journal of human genetics.

The G syndrome: a case report.

C. Greenberg, D. Schraufnagel, 1979, American journal of medical genetics.

Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome.

K. Entian, P. Cattini, C. Greenberg, 2009, American journal of human genetics.

New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians.

C. Greenberg, A. Chudley, T. Persaud, 1992, American journal of medical genetics.

Germline mosaicism in a female who seemed to be a carrier by sequence analysis.

S. Sommer, C. Greenberg, R. Ketterling, 1995, Human molecular genetics.

Population-Based Screening for Severe Combined Immunodeficiency in Manitoba, Canada

J. Thompson, C. Greenberg, T. Zelinski, 2018 .

Meckel syndrome in the Hutterite population is actually a Joubert‐related cerebello‐oculo‐renal syndrome

K. Boycott, F. Bernier, A. Innes, 2007, American journal of medical genetics. Part A.

Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1-16.3.

M. Hayden, C. Greenberg, D. Kalousek, 1986, American journal of human genetics.

Heterozygosity for a large deletion in the alpha 2(I) collagen gene has a dramatic effect on type I collagen secretion and produces perinatal lethal osteogenesis imperfecta.

P. Byers, K. Holbrook, C. Greenberg, 1988, The Journal of biological chemistry.

GLUT1 Deficiency Without Epilepsy: Yet Another Case

C. Greenberg, Charuta N. Joshi, D. D. De Vivo, 2008, Journal of child neurology.

LC-MS/MS progress in newborn screening.

C. Greenberg, D. Lehotay, P. Hall, 2011, Clinical biochemistry.

Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci.

C. Greenberg, W. Halliday, T. Weiler, 1997, American journal of medical genetics.

Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I

C. Greenberg, P. Frosk, M. R. Bigio, 2005, European Journal of Human Genetics.

Compound heterozygosity in the glutaryl-CoA dehydrogenase gene with R227P mutation in one allele is associated with no or very low free glutarate excretion

H. Leffers, M. Durán, M. Schwartz, 1997, Journal of Inherited Metabolic Disease.

Glutaryl‐CoA dehydrogenase mutations in glutaric acidemia (type I): Review and report of thirty novel mutations

M. Schwartz, C. Greenberg, E. Christensen, 1998, Human mutation.

Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysis.

A. Duncan, C. Greenberg, S. Goodman, 1994, Genomics.

Maintenance treatment of glutaryl-CoA dehydrogenase deficiency

K. Strauss, C. Greenberg, S. Kölker, 2004, Journal of Inherited Metabolic Disease.

Fibular aplasia with ectrodactyly.

C. Greenberg, M. Reed, J. Evans, 2002, American journal of medical genetics.

Paracentric inversion 11q in Canadian Hutterites

C. Greenberg, A. Chudley, B. Chodirker, 1992, Human Genetics.

Type I Gaucher disease following chemotherapy for light chain multiple myeloma.

W. Cheung, C. Greenberg, M. Seftel, 2007, Internal medicine.

An intronic polymorphism of the hMLH1 gene contributes toward incomplete genetic testing for HNPCC.

S. Andrew, C. Greenberg, E. Spriggs, 2002, Genetic testing.

Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene: Relevance for Other Adult-Onset Disorders

M. Hayden, W. Meschino, O. Suchowersky, 1993 .

Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds

P. Goodfellow, S. Gorski, C. Greenberg, 1994, Human Genetics.

Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.

C. Greenberg, A. Chudley, A. Innes, 2001, American journal of medical genetics.

Experiences of caregivers of children with inherited metabolic diseases: a qualitative study

John J. Mitchell, J. Little, K. Wilson, 2016, Orphanet Journal of Rare Diseases.

A Case Series and Review of CDKL5 Deficiency Disorder: More than Rett

J. Appendino, J. N. Hartley, C. Greenberg, 2020 .

Ketogenic diet in Alpers-Huttenlocher syndrome.

M. S. Salman, C. Greenberg, Charuta N. Joshi, 2009, Pediatric neurology.

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.

Colin A. Johnson, C. Ober, R. Hegele, 2011, American journal of human genetics.

Neuropathological Findings in Eight Children with Cerebro‐oculo‐facio‐skeletal (COFS) Syndrome

E. Zackai, L. Rorke, R. Schnur, 1997, Journal of neuropathology and experimental neurology.

Improved predictive carrier testing for familial adenomatous polyposis using DNA from a single archival specimen and polymorphic markers with multiple alleles.

C. Greenberg, B. Bapat, A. Mitri, 1993, Human pathology.

A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1.

M. Stratton, G. Bignell, W. Foulkes, 2001, The Journal of clinical endocrinology and metabolism.

The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein

C. Greenberg, N. K. Björklund, B. Chodirker, 2004, Reproductive biology and endocrinology : RB&E.

Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review

John J. Mitchell, L. Korngut, M. Taljaard, 2020, Orphanet Journal of Rare Diseases.

Ultrastructural abnormalities in bone and calcifying cartilage in two siblings with a newly described recessive lethal chondrodysplasia.

D. Rimoin, C. Greenberg, H. Gruber, 1990, Ultrastructural Pathology.

Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women.

B. Schmidt, D. Allingham-Hawkins, C. Greenberg, 2002, Neurology.

Bowen–Conradi syndrome: A clinical and genetic study

F. Bernier, A. Innes, C. Greenberg, 2003, American journal of medical genetics. Part A.

Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants.

J. Hamerton, C. Greenberg, J. Evans, 1986, Birth defects original article series.

Leu‐676‐Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred

D. Belsham, C. Greenberg, S. Liao, 1995, Human mutation.

Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

D. Belsham, C. Greenberg, W. Yee, 1992, Journal of the Neurological Sciences.

Erratum: Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm

M. Hayden, B. Kremer, S. Andrew, 1994, Nature Genetics.

Comparison of iodine-123-epidepride and iodine-123-IBZM for dopamine D2 receptor imaging.

W. Leslie, D. Hobson, C. Greenberg, 1996, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Clinical deficits in Huntington disease correlate with reduced striatal uptake on iodine-123 epidepride single-photon emission tomography

W. Leslie, C. Greenberg, D. Hobson, 1999, European Journal of Nuclear Medicine.

Spontaneous resolution of a cystic hygroma in a fetus with Turner syndrome

C. Greenberg, B. Chodirker, C. Harman, 1988, Prenatal diagnosis.

Isolated sulfite oxidase deficiency: a founder mutation

C. Greenberg, C. Prasad, E. Spriggs, 2020, Cold Spring Harbor molecular case studies.

Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria

John J. Mitchell, L. Korngut, M. Taljaard, 2021, Pediatrics.

Long‐term survival and normal cognitive development in infantile phosphofructokinase‐1 deficiency

C. Greenberg, E. Spriggs, S. Marles, 1999, Clinical genetics.

Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy.

C. Greenberg, J. Evans, K. Wrogemann, 1993, Journal of medical genetics.

A simple screening test for fatty acid oxidation defects using whole-blood palmitate oxidation

C. Greenberg, L. Dilling, L. Seargeant, 1999, Journal of Inherited Metabolic Disease.

The BOR syndrome and renal agenesis‐prenatal diagnosis andfurther clinical delineation

C. Greenberg, C. Trevenen, J. Evans, 1988, Prenatal Diagnosis.

The C 677 T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein

C. Greenberg, N. K. Björklund, B. Chodirker, 2015 .

Genetic Counseling in a Busy Pediatric Metabolic Practice

J. N. Hartley, C. Greenberg, A. Mhanni, 2011, Journal of Genetic Counseling.

Absence of chromosomal instability in one kindred with multiple endocrine neoplasia type 2A.

A. Duncan, C. Greenberg, 1986, Cancer genetics and cytogenetics.

Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria

W. Foulkes, Y. Butterfield, C. Caldas, 2004, Journal of Medical Genetics.

Low MSAFP levels and Williams syndrome.

C. Greenberg, A. Chudley, J. Evans, 1997, American journal of medical genetics.

Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973.

J. Hamerton, C. Greenberg, J. Evans, 1990, Birth defects original article series.

Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

I. Harting, C. Greenberg, J. Zschocke, 2017, Journal of Inherited Metabolic Disease.

Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening.

M. Cheang, C. Greenberg, J. Evans, 1990, American journal of human genetics.

Chondro‐osseous changes in cerebro‐oculo‐facial‐skeletal (COFS) syndrome

C. Greenberg, M H Reed, W S Hwang, 1982, The Journal of pathology.

Evolutionary Comparison Provides Evidence for Pathogenicity of RMRP Mutations

A. Reymond, E. Dermitzakis, C. Ucla, 2005, PLoS genetics.