FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Anne Spence

Research Profile

Disorders

Concepts & Ideas

Procedures

Chromosome Mapping

Physiology

Genes & Molecular Sequences

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Moyra Smith; M Anne Spence; Kimberley Verrell; Pamela L Flodman; John J Gargus; Richard Haas; Robert Naviaux; Katherine Osann; Gail E Reiner; Mariella T Simon; Douglas C Wallace
Mitochondrial and ion channel gene alterations in autism.
Moyra Smith; M Anne Spence; Pamela Flodman
Nuclear and mitochondrial genome defects in autisms.
Wendy A Goldberg; Kara L Thorsen; Kathryn Osann; M Anne Spence
Use of home videotapes to confirm parental reports of regression in autism.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Anne Spence (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Moyra Smith; M Anne Spence; Kimberley Verrell; Pamela L Flodman; John J Gargus; Richard Haas; Robert Naviaux; Katherine Osann; Gail E Reiner; Mariella T Simon; Douglas C Wallace
Mitochondrial and ion channel gene alterations in autism.
Biochimica et biophysica acta 2012;1817(10):1796-802.
2009: Moyra Smith; M Anne Spence; Pamela Flodman
Nuclear and mitochondrial genome defects in autisms.
Annals of the New York Academy of Sciences 2009;1151():102-32.
2008: Wendy A Goldberg; Kara L Thorsen; Kathryn Osann; M Anne Spence
Use of home videotapes to confirm parental reports of regression in autism.
Journal of autism and developmental disorders 2008;38(6):1136-46.
2008: Kara L Thorsen; Wendy A Goldberg; Kathryn Osann; M Anne Spence
Birthday and non-birthday videotapes: the importance of context for the behavior of young children with autism.
Journal of autism and developmental disorders 2008;38(6):1047-58.
2008: Katherine Gotham; Susan Risi; Geraldine Dawson; Helen Tager-Flusberg; Robert Joseph; Alice Carter; Susan Hepburn; William M McMahon; Patricia Rodier; Susan L Hyman; Marian Sigman; Sally J Rogers; Rebecca Landa; M Anne Spence; Kathryn Osann; Pamela Flodman; Fred Volkmar; Eric Hollander; Joseph Buxbaum; Andrew Pickles; Catherine Lord
A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithms.
Journal of the American Academy of Child and Adolescent Psychiatry 2008;47(6):642-51.
2008: Leslie Richter; Pamela Flodman; Fernando Barria von-Bischhoffshausen; Douglas Burch; Sandra Brown; Linda Nguyen; Julia Turner; M Anne Spence; J Bronwyn Bateman
Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA).
American journal of medical genetics. Part A 2008;146(7):833-42.
2007: J Bronwyn Bateman; Fernando R Barria von-Bischhoffshaunsen; Leslie Richter; Pamela Flodman; Douglas Burch; M Anne Spence
Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.
Ophthalmology 2007;114(3):425-32.
2006: Jenifer Juranek; Pauline A Filipek; Gholam R Berenji; Charlotte Modahl; Kathryn Osann; M Anne Spence
Association between amygdala volume and anxiety level: magnetic resonance imaging (MRI) study in autistic children.
Journal of child neurology 2006;21(12):1051-8.
2006: Janet E Lainhart; Erin D Bigler; Maureen Bocian; Hilary Coon; Elena Dinh; Geraldine Dawson; Curtis K Deutsch; Michelle A Dunn; Annette Estes; Helen Tager-Flusberg; Susan E Folstein; Susan Hepburn; Susan Hyman; William M McMahon; Nancy J Minshew; Jeffrey Munson; Kathryn Osann; Sally Ozonoff; Patricia M Rodier; Sally J Rogers; Marian Sigman; M Anne Spence; Stodgell Christopher; Fred Volkmar
Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism.
American journal of medical genetics. Part A 2006;140(21):2257-74.
2006: Gerard D Schellenberg; Geraldine Dawson; Yun Ju Sung; Annette Estes; Jeffrey Munson; E Rosenthal; J Rothstein; Pamela Flodman; Moyra Smith; Hilary Coon; L Leong; Chang-En Yu; Stodgell Christopher; Patricia M Rodier; M Anne Spence; Nancy J Minshew; William M McMahon; Ellen M Wijsman
Evidence for multiple loci from a genome scan of autism kindreds.
Molecular psychiatry 2006;11(11):1049-60, 979.
2006: J Bronwyn Bateman; Leslie Richter; Pamela Flodman; Douglas Burch; Sandra Brown; Philip Penrose; Otis Paul; David D Geyer; David G Brooks; M Anne Spence
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
Investigative ophthalmology & visual science 2006;47(8):3441-9.
2006: Jennifer Richler; Rhiannon Luyster; Susan Risi; Wan-Ling Hsu; Geraldine Dawson; Raphael Bernier; Michelle A Dunn; Susan Hepburn; Susan L Hyman; William M McMahon; Julie Goudie-Nice; Nancy J Minshew; Sally J Rogers; Marian Sigman; M Anne Spence; Wendy A Goldberg; Helen Tager-Flusberg; Fred Volkmar; Catherine Lord
Is there a 'regressive phenotype' of Autism Spectrum Disorder associated with the measles-mumps-rubella vaccine? A CPEA Study.
Journal of autism and developmental disorders 2006;36(3):299-316.
2006: Cynthia A Molloy; Ardythe L Morrow; Jareen Meinzen-Derr; Geraldine Dawson; Raphael Bernier; Michelle A Dunn; Susan L Hyman; William M McMahon; Julie Goudie-Nice; Susan Hepburn; Nancy J Minshew; Sally J Rogers; Marian Sigman; M Anne Spence; Helen Tager-Flusberg; Fred Volkmar; Catherine Lord
Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study.
Journal of autism and developmental disorders 2006;36(3):317-24.
2006: David D Geyer; M Anne Spence; Meriam Johannes; Pamela Flodman; Kevin Clancy; Rebecca Berry; Robert S Sparkes; Matthew D Jonsen; Sherwin J Isenberg; J Bronwyn Bateman
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.
American journal of ophthalmology 2006;141(4):761-3.
2005: Bernie Devlin; Edwin H Cook; Hilary Coon; Geraldine Dawson; Elena L Grigorenko; William M McMahon; Nancy J Minshew; David Pauls; Moyra Smith; M Anne Spence; Patricia M Rodier; Stodgell Christopher; Gerard D Schellenberg
Autism and the serotonin transporter: the long and short of it.
Molecular psychiatry 2005;10(12):1110-6.
2005: Wendy A Goldberg; Kelly L Jarvis; Kathryn Osann; Tracy M Laulhere; Carol Straub; Erin Thomas; Pauline A Filipek; M Anne Spence
Brief report: early social communication behaviors in the younger siblings of children with autism.
Journal of autism and developmental disorders 2005;35(5):657-64.
2005: Deborah L Grady; A Harxhi; k tejaswini; Pamela Flodman; M Anne Spence; James M Swanson; Robert K Moyzis
Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):33-5.
2005: Thomas H Wassink; Joseph Piven; Veronica J Vieland; Laura Jenkins; Rebecca Frantz; Christopher W Bartlett; Rhinda Goedken; Deb Childress; M Anne Spence; Moyra Smith; Val C Sheffield
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):36-44.
2005: Patrick W L Leung; Chi-chiu Lee; Se-fong Hung; Ting-Pong Ho; Chun-pan Tang; Shi-leung Kwong; S Y Leung; S T Yuen; Felice Lieh-Mak; Jaap Oosterlaan; Deborah L Grady; Ante Harxhi; Yuan-Chun Ding; Han-Chang Chi; Pamela Flodman; Sabrina Schuck; M Anne Spence; Robert K Moyzis; James Swanson
Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;133B(1):54-6.
2005: Mark W Logue; Andrew W George; M Anne Spence; Veronica J Vieland
Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations.
BMC genetics 2005;6 Suppl 1():S141.
2005: Rhiannon Luyster; Jennifer Richler; Susan Risi; Wan-Ling Hsu; Geraldine Dawson; Raphael Bernier; Michelle A Dunn; Susan Hepburn; Susan L Hyman; William M McMahon; Julie Goudie-Nice; Nancy J Minshew; Sally J Rogers; Marian Sigman; M Anne Spence; Wendy A Goldberg; Helen Tager-Flusberg; Fred Volkmar; Catherine Lord
Early regression in social communication in autism spectrum disorders: a CPEA Study.
Developmental neuropsychology 2005;27(3):311-36.
2004: E Wang; Yuan-Chun Ding; Pamela Flodman; J R Kidd; Kenneth K Kidd; Deborah L Grady; Oliver Ryder; M Anne Spence; James M Swanson; Robert K Moyzis
The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.
American journal of human genetics 2004;74(5):931-44.
2004: Subhadra Ramanathan; Abigail Woodroffe; Pamela Flodman; Lee Z Mays; Mona Hanouni; Charlotte Modahl; Robin Steinberg-Epstein; Maureen Bocian; M Anne Spence; Moyra Smith
A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.
BMC medical genetics 2004;5():10.
2004: Sally Ozonoff; Ian Cook; Hilary Coon; Geraldine Dawson; Robert M Joseph; Ami Klin; William M McMahon; Nancy J Minshew; Jeffrey Munson; Bruce F Pennington; Sally J Rogers; M Anne Spence; Helen Tager-Flusberg; Fred Volkmar; Debora Wrathall
Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network.
Journal of autism and developmental disorders 2004;34(2):139-50.
2004: Bernie Devlin; Pamela Bennett; Geraldine Dawson; Denise A Figlewicz; Elena L Grigorenko; William M McMahon; Nancy J Minshew; David Pauls; Moyra Smith; M Anne Spence; Patricia M Rodier; Stodgell Christopher; Gerard D Schellenberg
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):46-50.
2004: Carrie E Haverty; Angela E Lin; Ellen Simpson; M Anne Spence; Rick A Martin
47,XXX associated with malformations.
American journal of medical genetics. Part A 2004;125A(1):108-11; author reply 112.
2003: Wendy A Goldberg; Kathryn Osann; Pauline A Filipek; Tracy M Laulhere; Kelly L Jarvis; Charlotte Modahl; Pamela Flodman; M Anne Spence
Language and other regression: assessment and timing.
Journal of autism and developmental disorders 2003;33(6):607-16.
2003: Pauline A Filipek; Jenifer Juranek; Moyra Smith; Lee Z Mays; Erica R Ramos; Maureen Bocian; Diane Masser-Frye; Tracy M Laulhere; Charlotte Modahl; M Anne Spence; J Jay Gargus
Mitochondrial dysfunction in autistic patients with 15q inverted duplication.
Annals of neurology 2003;53(6):801-4.
2003: Deborah L Grady; Han-Chang Chi; Yuan-Chun Ding; k tejaswini; E Wang; Sabrina Schuck; Pamela Flodman; M Anne Spence; James M Swanson; Robert K Moyzis
High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.
Molecular psychiatry 2003;8(5):536-45.
2003: M Anne Spence; David A Greenberg; Susan E Hodge; Veronica J Vieland
The emperor's new methods.
American journal of human genetics 2003;72(5):1084-7.
2003: Abraham A Palmer; Laura Breen; Pamela Flodman; Lisa H Conti; M Anne Spence; Morton P Printz
Identification of quantitative trait loci for prepulse inhibition in rats.
Psychopharmacology 2003;165(3):270-9.
2002: Bernie Devlin; Pamela Bennett; Edwin H Cook; Geraldine Dawson; David Gonen; Elena L Grigorenko; William M McMahon; David Pauls; Moyra Smith; M Anne Spence; Gerard D Schellenberg
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
American journal of medical genetics 2002;114(6):667-72.
2002: Katherine Neiswanger; Margaret E Cooper; Seth M Weinberg; Pamela Flodman; A Bundens Keglovits; Y Liu; Dan-Ning Hu; Michael Melnick; M Anne Spence; Mary L Marazita
Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population.
Orthodontics & craniofacial research 2002;5(3):140-6.
2002: Chang-En Yu; Geraldine Dawson; Jeffrey Munson; Ian D'Souza; Julie Osterling; Annette Estes; Anne-Louise Leutenegger; Pamela Flodman; Moyra Smith; Wendy H Raskind; M Anne Spence; William M McMahon; Ellen M Wijsman; Gerard D Schellenberg
Presence of large deletions in kindreds with autism.
American journal of human genetics 2002;71(1):100-15.
2002: Rebecca L Jaworski; Martin Jirout; Shamara Closson; Laura Breen; Pamela Flodman; M Anne Spence; Vladimír Kren; Drahomira Krenova; Michal Pravenec; Morton P Printz
Heart rate and blood pressure quantitative trait loci for the airpuff startle reaction.
Hypertension 2002;39(2 Pt 2):348-52.
2002: Yuan-Chun Ding; Han-Chang Chi; Deborah L Grady; Atsuyuki Morishima; Judith R Kidd; Kenneth K Kidd; Pamela Flodman; M Anne Spence; Sabrina Schuck; James M Swanson; Ya-Ping Zhang; Robert K Moyzis
Evidence of positive selection acting at the human dopamine receptor D4 gene locus.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(1):309-14.
2002: Moyra Smith; A Woodroffe; R Smith; S Holguin; J Martinez; Pauline A Filipek; Charlotte Modahl; B Moore; Maureen Bocian; Lee Z Mays; Tracy M Laulhere; Pamela Flodman; M Anne Spence
Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.
Cytogenetic and genome research 2002;98(4):233-9.
2001: Susan L Slager; T Foroud; faride haghighi; M Anne Spence; Susan E Hodge
Stoppage: an issue for segregation analysis.
Genetic epidemiology 2001;20(3):328-39.
2001: John R Kelsoe; M Anne Spence; E Loetscher; M Foguet; A Dessa Sadovnick; Ronald A Remick; Pamela Flodman; J Khristich; Z Mroczkowski-Parker; J L Brown; D Masser; S Ungerleider; Mark Hyman Rapaport; W L Wishart; H Luebbert
A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(2):585-90.
2001: Pamela Flodman; Anthony J Macula; M Anne Spence; D C Torney
Preliminary implementation of new data mining techniques for the analysis of simulation data from Genetic Analysis Workshop 12: problem 2.
Genetic epidemiology 2001;21 Suppl 1():S390-5.
2001: Moyra Smith; J R Escamilla; Pauline A Filipek; Maureen Bocian; Charlotte Modahl; Pamela Flodman; M Anne Spence
Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.
Cytogenetics and cell genetics 2001;94(1-2):15-22.
2000: Moyra Smith; Pauline A Filipek; C Wu; Maureen Bocian; S Hakim; Charlotte Modahl; M Anne Spence
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.
American journal of medical genetics 2000;96(6):765-70.
2000: J Bronwyn Bateman; David D Geyer; Pamela Flodman; Meriam Johannes; James M Sikela; Nicole Walter; A T Moreira; Kevin Clancy; M Anne Spence
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
Investigative ophthalmology & visual science 2000;41(11):3278-85.
2000: J Bronwyn Bateman; Meriam Johannes; Pamela Flodman; David D Geyer; Kevin Clancy; C Heinzmann; T Kojis; Rebecca Berry; Robert S Sparkes; M Anne Spence
A new locus for autosomal dominant cataract on chromosome 12q13.
Investigative ophthalmology & visual science 2000;41(9):2665-70.
2000: James Swanson; Jaap Oosterlaan; M Murias; Sabrina Schuck; Pamela Flodman; M Anne Spence; Michael Wasdell; Y Ding; Han-Chang Chi; k tejaswini; M Mann; C Carlson; James L Kennedy; J A Sergeant; P Leung; Y P Zhang; A Sadeh; C Chen; Carol K Whalen; K A Babb; Robert K Moyzis; M I Posner
Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(9):4754-9.
2000: R A Martin; V Hunter; W Neufeld-Kaiser; Pamela Flodman; M Anne Spence; D Furnas; K A Martin
Ultrasonographic detection of orbicularis oris defects in first degree relatives of isolated cleft lip patients.
American journal of medical genetics 2000;90(2):155-61.
2000: James M Swanson; Pamela Flodman; J Kennedy; M Anne Spence; Robert K Moyzis; Sabrina Schuck; M Murias; J Moriarity; C Barr; k tejaswini; M Posner
Dopamine genes and ADHD.
Neuroscience and biobehavioral reviews 2000;24(1):21-5.
1999: S E Hodge; M Boehnke; M Anne Spence
Loss of information due to ambiguous haplotyping of SNPs.
Nature genetics 1999;21(4):360-1.
1999: D A Greenberg; J W MacCluer; M Anne Spence; Catherine T Falk; Susan E Hodge
Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and why.
Genetic epidemiology 1999;17 Suppl 1():S449-59.
1998: Susan E Hodge; Pamela Flodman; M F Duryea; M Anne Spence
Estimating recombination fraction separately for males and females: a counterintuitive result.
Human heredity 1998;48(1):42-8.
1998: D A Greenberg; Susan E Hodge; Veronica J Vieland; M Anne Spence
Power, mode of inheritance, and type I error in LOD scores and affecteds-only methods: reply to Kruglyak.
American journal of human genetics 1998;62(1):202-4.
1997: Roza Hayduk; Pamela Flodman; M Anne Spence; M K Erman; Merrill M. Mitler
HLA haplotypes, polysomnography, and pedigrees in a case series of patients with narcolepsy.
Sleep 1997;20(10):850-7.
1997: JD McPherson; B Apostol; C B Wagner-McPherson; S Hakim; R G Del Mastro; N Aziz; E Baer; G Gonzales; M C Krane; R Markovich; Peter S Masny; M Ortega; J Vu; M Vujicic; D M Church; A Segal; D L Grady; Robert K Moyzis; M Anne Spence; Michael Lovett; JJ Wasmuth
A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.
Genome research 1997;7(9):897-909.
1997: J P Homer; Pamela Flodman; M Anne Spence
Bipolar disorder: dominant or recessive on chromosome 5?
Genetic epidemiology 1997;14(6):647-51.
1996: John R Kelsoe; A D Sadovnick; H Kristbjarnarson; P Bergesch; Z Mroczkowski-Parker; M Drennan; Mark Hyman Rapaport; Pamela Flodman; M Anne Spence; R A Remick
Possible locus for bipolar disorder near the dopamine transporter on chromosome 5.
American journal of medical genetics 1996;67(6):533-40.
1996: John R Kelsoe; R A Remick; A D Sadovnick; H Kristbjarnarson; Pamela Flodman; M Anne Spence; M Morison; Z Mroczkowski-Parker; P Bergesch; Mark Hyman Rapaport; A L Mirow; Randy D Blakely; T Helgason; Janice A Egeland
Genetic linkage study of bipolar disorder and the serotonin transporter.
American journal of medical genetics 1996;67(2):215-7.
1996: T L Kojis; C Heinzmann; Pamela Flodman; J T Ngo; RS Sparkes; M Anne Spence; J B Bateman; John R Heckenlively
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.
American journal of human genetics 1996;58(2):347-55.
1995: M Anne Spence; Pamela Flodman; A D Sadovnick; J E Bailey-Wilson; H Ameli; R A Remick
Bipolar disorder: evidence for a major locus.
American journal of medical genetics 1995;60(5):370-6.
1994: F L Munier; L Arabien; Pamela Flodman; M Anne Spence; G Pescia; H P Rutz; A L Murphree
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees.
Human genetics 1994;94(5):484-90.
1993: F L Munier; Ming X Wang; M Anne Spence; Francine Thonney; Aubin Balmer; G Pescia; L A Donoso; A L Murphree
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees.
Archives of ophthalmology 1993;111(11):1507-11.
1993: J B Bateman; T L Kojis; R M Cantor; C Heinzmann; J T Ngo; M Anne Spence; George Inana; J D Kivlin; D Curtis; RS Sparkes
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.
Transactions of the American Ophthalmological Society 1993;91():299-307; discussion 307-8.
1992: F Munier; M Anne Spence; G Pescia; Aubin Balmer; C Gailloud; Francine Thonney; G van Melle; H P Rutz
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene.
Human genetics 1992;89(5):508-12.
1990: J T Ngo; J B Bateman; M Anne Spence; V Cortessis; RS Sparkes; J D Kivlin; T Mohandas; George Inana
Ornithine aminotransferase (OAT): recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus.
Genomics 1990;6(1):123-8.
1989: A M Goldstein; Robert W Haile; M Anne Spence; RS Sparkes; Annlia Paganini-Hill
A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. II. Linkage analysis.
Clinical genetics 1989;36(2):100-6.
1989: J Ngo; M Anne Spence; V Cortessis; J B Bateman; RS Sparkes
Duplicate report crossing over in Norrie disease family.
American journal of medical genetics 1989;33(2):286.
1989: J T Ngo; J B Bateman; V Cortessis; RS Sparkes; T Mohandas; George Inana; M Anne Spence
Norrie disease: linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe.
Genomics 1989;4(4):539-45.
1988: J T Ngo; M Anne Spence; V Cortessis; RS Sparkes; J B Bateman
Recombinational event between Norrie disease and DXS7 loci.
Clinical genetics 1988;34(1):43-7.
1988: A M Goldstein; R W Haile; Susan E Hodge; A Paganini-Hill; M Anne Spence
Possible heterogeneity in the segregation pattern of breast cancer in families with bilateral breast cancer.
Genetic epidemiology 1988;5(2):121-33.
1988: K O'Hanlon; K Weissbecker; V Cortessis; M Anne Spence; E A Azen
Genes for salivary proline-rich proteins and taste for phenylthiourea are not closely linked in humans.
Cytogenetics and cell genetics 1988;49(4):315-7.
1987: M Anne Spence; RS Sparkes; D M Parry; S J Bale; V Cortessis; J J Mulvihill
Genetic linkage studies with neurofibromatosis: the question of heterogeneity.
Journal of medical genetics 1987;24(9):527-9.