C. Anderson

发表

Metabolic and Underlying Causes of Diabetes Mellitus

Å. Lernmark, F. Matschinsky, G. Grodsky, 1982, Diabetes.

Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis

E. Zackai, K. Gripp, W. Dobyns, 2013, American journal of medical genetics. Part A.

Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18

V. Huff, J. de Chadarévian, H. Punnett, 2003, American journal of medical genetics. Part A.

HLA Genotypic Study of Insulin-dependent Diabetes: The Excess of DR3/DR4 Heterozygotes Allows Rejection of the Recessive Hypothesis

J. Rotter, D. Rimoin, P. Terasaki, 1983, Diabetes.

Transposition of the great arteries in a neonate with Klinefelter syndrome—An incidental finding or a true association

N. Obiri, A. Moulick, S. Ge, 2015, American journal of medical genetics. Part A.

Hereditary considerations in common disorders.

J. Rotter, J. Zonana, C. Anderson, 1978, Pediatric clinics of North America.

The natural history of euploid pregnancies with first-trimester cystic hygromas.

A. Johnson, S. Heeger, C. Anderson, 1994, American journal of obstetrics and gynecology.

Absence of WNT4 gene mutation in a patient with MURCS association

T. Ganguly, F. De Luca, C. Anderson, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Fraternal twins with autism, severe cognitive deficit, and epilepsy: diagnostic role of chromosomal microarray analysis.

J. Imitola, A. Legido, Diana J. Walleigh, 2014, Seminars in pediatric neurology.

Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome.

L. Jackson, R. Wallerstein, J. Hoyer, 1997, American journal of medical genetics.

A search for heterogeneity in insulin dependent diabetes mellitus (IDDM): HLA and autoimmune studies in simplex, multiplex and multigenerational families.

S. Hodge, D. Rimoin, P. Terasaki, 1983, Metabolism: clinical and experimental.

5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report

I. Valencia, A. Legido, H. Marks, 2010, Journal of child neurology.

Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.

L. Jackson, R. Wallerstein, C. Anderson, 1996, Journal of medical genetics.

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

Stephanie E. Vallee, J. Rosenfeld, R. Tervo, 2013, American journal of medical genetics. Part A.

Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome Xp

J. Morrissette, J. de Chadarévian, H. Punnett, 2009, Pediatric blood & cancer.

Spondylometepiphyseal dysplasia, Strudwick type.

D. Sillence, J. Dorst, D. Rimoin, 1982, American journal of medical genetics.

The gene for Bazex-Dupré-Christol syndrome maps to chromosome Xq.

G. Aubert, D. Lacombe, Pierre Vabres, 1995, The Journal of investigative dermatology.

Amniotic Fluid Concentrations of Δ5 and Δ4 Steroids in Fetuses with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency and in Anencephalic Fetuses

I. Merkatz, V. Riccardi, M. New, 1980 .

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

E. Zackai, E. Bermejo, B. Weschke, 2003, Journal of medical genetics.

Prenatal zidovudine use and congenital anomalies in a medicaid population.

W. Hauck, B. Turner, C. Newschaffer, 2000 .

Prenatal Zidovudine Use and Congenital Anomalies in a Medicaid Population

B. Turner, C. Newschaffer, C. Anderson, 2000, Journal of acquired immune deficiency syndromes.

The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.

S. Hodge, D. Rimoin, K. Neiswanger, 1983, American journal of human genetics.

A report of three patients with an interstitial deletion of chromosome 15q24

A. Cherry, O. Abdul-Rahman, G. Vance, 2005, American journal of medical genetics. Part A.

A syndrome of short stature, joint laxity and developmental delay

A. Walker, M. Bocian, R. Lachman, 1982, Clinical genetics.

TO JMG Characterisation of deletions of the ZFHX 1 B region and genotype-phenotype analysis in Mowat-Wilson syndrome

E. Zackai, B. Weschke, I. Temple, 2003 .

Amniotic fluid concentrations of delta 5 and delta 4 steroids in fetuses with congenital adrenal hyperplasia due to 21 hydroxylase deficiency and in anencephalic fetuses.

I. Merkatz, V. Riccardi, M. New, 1980, The Journal of clinical endocrinology and metabolism.

Association studies between type 1 (insulin-dependent) diabetes and 27 genetic markers: Lack of association between type 1 diabetes and kidd blood group

M. Spence, S. Hodge, J. Rotter, 1983, Diabetologia.

Co‐occurrence of non‐mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: Case report and review of the literature

H. Punnett, J. Pascasio, C. Anderson, 2014, American journal of medical genetics. Part A.

Ovine hereditary chondrodysplasia (spider syndrome) in Suffolk lambs.

C. Anderson, P. Phillips, C. Bunn, 1993, Australian veterinary journal.

Preferential transmission of diabetic alleles within the HLA gene complex.

J. Rotter, N. Maclaren, C. Vadheim, 1986, The New England journal of medicine.

Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

L. Jackson, R. Wallerstein, B. Hay, 1997, Journal of medical genetics.

Dubowitz syndrome in a boy without developmental delay: further evidence for phenotypic variability.

L. Jackson, R. Wallerstein, C. Anderson, 1997, American journal of medical genetics.

Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis.

T. Mohandas, J. Opitz, M. Kaback, 1985, American journal of medical genetics.

Microarray analysis in children with developmental disorder or epilepsy.

I. Valencia, A. Legido, H. Marks, 2010, Pediatric neurology.

No evidence for linkage between an insulin‐dependent diabetes mellitus‐susceptibility locus and immunoglobulin loci KM or GM

M. Spence, A. Goldstein, D. Rao, 1984, Genetic epidemiology.

Diabetes: Evidence from Pairs of Affected Siblings

M. Spence, L. Field, C. Anderson, 2006 .

Response to Correspondence on ‘‘5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report’’

I. Valencia, A. Legido, H. Marks, 2011 .

HLA-dependent GM effects in insulin-dependent diabetes: evidence from pairs of affected siblings.

M. Spence, J. Rotter, L. Field, 1986, American journal of human genetics.

The search for heterogeneity in insulin-dependent diabetes mellitus: evidence for familial and nonfamilial forms.

C. Anderson, D. Greenberg, 1983, American journal of medical genetics.

Glyoxalase I “null” allele in a new family: Identification by abnormal segregation pattern and quantitative assay

R. Sparkes, C. Anderson, M. Sparkes, 2004, Human Genetics.

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes

Stephanie E. Vallee, J. Rosenfeld, R. Tervo, 2013, American journal of medical genetics. Part A.