M. Sarfarazi

发表

Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin

R. Ritch, R. Hitchings, A. Child, 2002, Science.

Localization of the fourth locus (GLC1E) for adult-onset primary open-angle glaucoma to the 10p15-p14 region.

A. Child, G. Brice, R. Crick, 1998, American journal of human genetics.

Genetic prediction and family structure in Huntington's chorea.

P. Harper, M. Sarfarazi, 1985, British medical journal.

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, Human molecular genetics.

Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.

M. Sarfarazi, N. Akarsu, M. Barsoum-Homsy, 1995, Genomics.

The Third Genetic Locus (GLC3C) for Primary Congenital Glaucoma (PCG) Maps to Chromosome 14q24.3

M. Sarfarazi, I. Stoilov, 2002 .

Molecular genetics of primary congenital glaucoma in Brazil.

V. P. Costa, M. Sarfarazi, J. P. Vasconcellos, 2002, Investigative ophthalmology & visual science.

The role of the WDR36 gene on chromosome 5q22.1 in a large family with primary open-angle glaucoma mapped to this region.

P. Kramer, S. Monemi, M. Sarfarazi, 2006, Archives of ophthalmology.

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

J. Farnham, P. Harper, M. Upadhyaya, 1992, American journal of human genetics.

Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma

A. Tarkkanen, R. Ritch, C. O'brien, 2008, Molecular vision.

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

J. Allanson, P. Harper, M. Upadhyaya, 1991, Journal of medical genetics.

Molecular Genetics of Primary Open-Angle Glaucoma

A. Child, M. Sarfarazi, J. Aragon-Martin, 2012 .

Xenobiotic‐metabolizing Cytochromes P450 in Ontogeny: Evolving Perspective

J. Schenkman, D. Choudhary, M. Sarfarazi, 2004, Drug metabolism reviews.

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

M. Pericak-Vance, C. Wijmenga, K. Mathews, 1992, American journal of human genetics.

Enhanced expression of CYP1B1 in Escherichia coli.

J. Schenkman, M. Sarfarazi, I. Jansson, 2000, Toxicology.

Gene mapping and chromosome 19.

D. Shaw, P. Harper, M. Sarfarazi, 1986, Journal of medical genetics.

Cyp1b1 Protein in the Mouse Eye during Development: An Immunohistochemical Study

J. Schenkman, K. Rezaul, D. Choudhary, 2007, Drug Metabolism and Disposition.

Predictors of axial and peripheral bone mineral density in healthy children and adolescents, with special attention to the role of puberty.

G. Dalsky, P. Gendreau, M. Sarfarazi, 1993, The Journal of pediatrics.

Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.

C. Jackson, M. E. Hodes, P. Conneally, 1993, Connective tissue research.

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.

M. Sarfarazi, A. Akarsu, B. Şayli, 1996, Human molecular genetics.

Metabolism of retinoids and arachidonic acid by human and mouse cytochrome P450 1b1.

J. Schenkman, D. Choudhary, M. Sarfarazi, 2004, Drug metabolism and disposition: the biological fate of chemicals.

(synpolydactyly). 2 Homozygous phenotype?

M. Sarfarazi, U. Şaylı, O. Akhan, 2022 .

Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma

J. Schenkman, D. Choudhary, M. Sarfarazi, 2008, Pharmacogenetics and genomics.

Expression of cytochrome P 450 1 b 1 ( Cyp 1 b 1 ) during early murine development

J. Schenkman, T. Rezaie, M. Sarfarazi, 2004 .

Multiple synostosis type 2 (SYNS2) maps to 20q11.2 and caused by a missense mutation in the growth/differentiation factor 5 (GDF5).

T. Rezaie, M. Sarfarazi, D. Farhud, 1999 .

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.

K. Davies, R. Williamson, P. Harper, 1983, Nucleic acids research.

Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences.

K. Davies, R. Williamson, P. Harper, 1983, Journal of medical genetics.

Close flanking markers for neurofibromatosis type I (NF1).

P. Harper, M. Upadhyaya, A. Fryer, 1989, American journal of human genetics.

DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease

P. Harper, M. Upadhyaya, M. Owen, 1990, The Lancet.

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

M. Pericak-Vance, T. Siddique, M. Upadhyaya, 1989, Journal of medical genetics.

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

K. Burnand, S. Mansour, A. Child, 2002, Journal of medical genetics.

Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19

D. Shaw, P. Harper, G. Bell, 1986, Human Genetics.

Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.

A. Child, G. Brice, M. Sarfarazi, 1998, American journal of human genetics.

Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics.

M. Sarfarazi, J. Alvarado, D. Hollander, 2006, American journal of ophthalmology.

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

V. Ferák, M. Sarfarazi, M. Plášilová, 1999, Journal of medical genetics.

Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli.

M. Sarfarazi, C. Malchoff, F. Forouhar, 1999, Thyroid : official journal of the American Thyroid Association.

Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, American journal of medical genetics.

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.

M. Sarfarazi, N. Akarsu, U. Şaylı, 1995, Journal of medical genetics.

Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker.

M. Sarfarazi, A. Akarsu, B. Şayli, 1995, Human molecular genetics.

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21.

M. Sarfarazi, A. Akarsu, I. Stoilov, 1997, Human molecular genetics.

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil

V. P. Costa, M. B. de Melo, S. Senthil, 2015, PloS one.

Molecular cloning, genomic structure, and protein characterization of mouse optineurin.

T. Rezaie, M. Sarfarazi, 2005, Genomics.

Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.

C. L. Jackson, P. Harper, T. Glaser, 1988, Genomics.

Comparative expression profiling of 40 mouse cytochrome P450 genes in embryonic and adult tissues.

J. Schenkman, D. Choudhary, M. Sarfarazi, 2003, Archives of biochemistry and biophysics.

Canadian Ophthalmological Society evidence-based clinical practice guidelines for cataract surgery in the adult eye.

M. Steinbach, Andrew Lee, A. Wong, 2008, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Molecular genetics of primary congenital glaucoma

M. Sarfarazi, I. Stoilov, 2000, Eye.

Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

A. Child, P. Comeglio, G. Brice, 2003, Journal of medical genetics.

Cause of Primary Congenital Lymphedema

A. Child, M. Sarfarazi, J. Beninson, 1999, Angiology.

Mapping of primary congenital lymphedema to the 5q35.3 region.

V. Sotirova, K. Burnand, A. Child, 1999, American journal of human genetics.

LTBP2 gene analysis in the GLC3C-linked family and 94 CYP1B1-negative cases with primary congenital glaucoma

P. Khaw, A. Child, M. Sarfarazi, 2013, Ophthalmic genetics.

Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1.

R. Ritch, J. Liebmann, G. Spaeth, 2005, Human molecular genetics.

Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.

D. Viljoen, R. Devereux, B. Sykes, 1992, The New England journal of medicine.

Genotype and phenotype correlations in congenital glaucoma.

M. Sarfarazi, J. Alvarado, D. Hollander, 2006, Transactions of the American Ophthalmological Society.

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.

K. Marymee, A. Clarke, P. Harper, 1989, The Journal of pediatrics.

Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population.

P. Harper, F. Davies, G. Coles, 1987, Journal of medical genetics.

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

P. Harper, P. Pearson, H. Kingston, 1983, Journal of medical genetics.

Stepwise Differentiation of Retinal Ganglion Cells from Human Pluripotent Stem Cells Enables Analysis of Glaucomatous Neurodegeneration

M. Sarfarazi, T. Cummins, Jason S. Meyer, 2016, Stem cells.

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

M. Sarfarazi, U. Şaylı, O. Akhan, 1995, Journal of medical genetics.

A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

M. Owen, P. Harper, M. Upadhyaya, 1991, Journal of medical genetics.

Linkage analysis in Marfan syndrome.

S. Blanton, M. Sarfarazi, P. Tsipouras, 1990, Journal of medical genetics.

A gene for lymphedema-distichiasis maps to 16q24.3.

A. Sigurdsson, M. Stratton, N. Rahman, 1999, American journal of human genetics.

Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome.

A. Arnold, M. Sarfarazi, V. Joshi, 2000, The Journal of clinical endocrinology and metabolism.

Roles of Cytochrome P450 in Development

J. Schenkman, M. Sarfarazi, I. Stoilov,, 2001, Drug metabolism and drug interactions.

Genetics and biochemistry of primary congenital glaucoma.

J. Schenkman, M. Sarfarazi, I. Stoilov, 2003, Ophthalmology clinics of North America.

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

M. Mattei, Brendan H. Lee, E. Vitale, 1991, Nature.

Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2

K. Burnand, S. Mansour, A. Child, 2008, European Journal of Human Genetics.

Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations

Alberto Smith, K. Burnand, S. Mansour, 2005, Human Genetics.

Physiological Significance and Expression of P450s in the Developing Eye

J. Schenkman, D. Choudhary, M. Sarfarazi, 2006, Drug metabolism reviews.

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.

D. Shaw, P. Harper, M. Sarfarazi, 1986, British medical journal.

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

P. Harper, L. Elsas, M. Sarfarazi, 1986, Journal of medical genetics.

Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region.

A. Child, R. Crick, M. Sarfarazi, 1996, Genomics.

Recent advances in molecular genetics of glaucomas.

M Sarfarazi, M. Sarfarazi, 1997, Human molecular genetics.

Milroy disease and the VEGFR-3 mutation phenotype

K. Burnand, S. Mansour, A. Child, 2005, Journal of Medical Genetics.

Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma model

M. Walter, M. Sarfarazi, S. Dubois, 2011, Molecular vision.

Defining the pathogenicity of optineurin in juvenile open-angle glaucoma.

Y. Buys, G. Trope, C. Willoughby, 2004, Investigative ophthalmology & visual science.

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

B. Tusi, M. Sadeghi, E. Elahi, 2007, The Journal of molecular diagnostics : JMD.

Roles of CYP1B1, Optineurin, and WDR36 Gene Mutations in Glaucoma

J. Schenkman, D. Choudhary, S. Monemi, 2008 .

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

P. Harper, M. Upadhyaya, M. Sarfarazi, 1986, Human Genetics.

Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.

P. Harper, M. Upadhyaya, M. Sarfarazi, 1989, Journal of medical genetics.

A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study.

C Junien, M Sarfarazi, P Farndon, 1992, Journal of medical genetics.

Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.

M. Sarfarazi, B. Weiffenbach, P. Tsipouras, 1991, Proceedings of the National Academy of Sciences of the United States of America.

An exclusion map of Marfan syndrome.

L. Peltonen, J. de Groote, H. Eiberg, 1990, Journal of medical genetics.

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy

D. Shaw, P. Harper, M. Sarfarazi, 1990, Human Genetics.

Genetic linkage relationships between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy

K. Davies, R. Williamson, P. Harper, 2004, Human Genetics.

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

K. Davies, R. Williamson, P. Harper, 1983, Journal of medical genetics.

Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19

T. Wienker, M. Koch, B. Zoll, 1989, Human Genetics.

Effect of two mutations of human CYP1B1, G61E and R469W, on stability and endogenous steroid substrate metabolism.

J. Schenkman, M. Sarfarazi, I. Jansson, 2001, Pharmacogenetics.

Optineurin in primary open angle glaucoma.

T. Rezaie, M. Sarfarazi, 2003, Ophthalmology clinics of North America.

X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization

A. Clarke, P. Harper, M. Sarfarazi, 1987, Human Genetics.

Studies of a DNA marker (G8) genetically linked to Huntington disease in British families

R. Tanzi, J. Gusella, S. Youngman, 1986, Human Genetics.

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy

L. Kunkel, K. Davies, D. Shaw, 2004, Human Genetics.

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

P. Harper, H. Kingston, M. Sarfarazi, 2004, Human Genetics.

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

K. Marymee, A. Clarke, P. Harper, 1988, American journal of human genetics.

Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.

S. Youngman, D. Shaw, P. Harper, 1985, Journal of medical genetics.

Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.

D. Shaw, P. Harper, P. Pearson, 1985, Journal of medical genetics.

Refinement of the locus for autosomal dominant juvenile optic atrophy to a 2 cM region on 3q28.

A. Child, M. Sarfarazi, D. Stoilova, 1997, Ophthalmic genetics.

Expression patterns of mouse and human CYP orthologs (families 1-4) during development and in different adult tissues.

J. Schenkman, D. Choudhary, M. Sarfarazi, 2005, Archives of biochemistry and biophysics.

Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population.

A. Bakkaloğlu, S. Ozen, M. Sarfarazi, 1997, Journal of medical genetics.

Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene.

S. Bhattacharya, T. Aung, R. Hitchings, 2005, Investigative ophthalmology & visual science.

A third locus (GLC1D) for adult-onset primary open-angle glaucoma maps to the 8q23 region.

E. Traboulsi, M. Sarfarazi, D. Stoilova, 1998, American journal of ophthalmology.

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements.

C. Wijmenga, J. Farnham, P. Harper, 1993, Human molecular genetics.

Common Molecular Challenges in Glaucoma

M. Sarfarazi, 2015, Journal of ophthalmic & vision research.

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

R. Mcinnes, A. Duncan, E. Percin, 2000, Nature Genetics.

Identification of a new 'TIGR' mutation in a family with juvenile-onset primary open angle glaucoma.

A. Child, G. Brice, R. Crick, 1997, Ophthalmic genetics.

NovelTIGR/MYOCmutations infamilies with juvenile onsetprimary open angle glaucoma

R. Crick, M. Sarfarazi, D. Stoilova, 2011 .

Novel TIGR/MYOC mutations in families with juvenile onset primary open angle glaucoma.

A. Child, H. Garchon, M. Adam, 1998, Journal of medical genetics.

A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes.

P. Harper, M. Upadhyaya, M. Sarfarazi, 1989, Journal of medical genetics.

Molecular cloning and expression profiling of optineurin in the rhesus monkey.

P. Kaufman, D. Waitzman, T. Rezaie, 2005, Investigative ophthalmology & visual science.

Expression of cytochrome P4501b1 (Cyp1b1) during early murine development.

J. Schenkman, T. Rezaie, M. Sarfarazi, 2004, Molecular Vision.

Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14

P. Harper, M. Upadhyaya, M. Sarfarazi, 1988, Journal of the Neurological Sciences.

Linkage analysis oftwodonedDNA sequences flanking theDuchenne muscular dystrophy locus on theshort armofthehumanX chromosome

K. Davies, R. Williamson, P. Harper, 1983 .

Analysis of Rare Variants and Common Haplotypes in the Optineurin Gene in Swedish Glaucoma Cases

C. Wadelius, T. Rezaie, M. Sarfarazi, 2005, Ophthalmic genetics.

Evidence against Linkage of von Recklinghausen Neurofibromatosis and Chromosome 19 Markers

D. Shaw, M. Sarfarazi, A. Meredith, 1986, Annals of the New York Academy of Sciences.

Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.

D. Shaw, P. Harper, M. Sarfarazi, 1986, Journal of medical genetics.

A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.

M Sarfarazi, M. Bucan, S. Youngman, 1989, Genomics.

PRENATAL DIAGNOSIS OF DUCHENNE DYSTROPHY

HywelC. Williams, P. Harper, M. Sarfarazi, 1985, The Lancet.

Chromosome 17 markers and von Recklinghausen neurofibromatosis: a genetic linkage study in a British population.

P. Harper, M. Upadhyaya, K. Stephens, 1987, Genomics.

Genome-wide association study in primary angle closure glaucoma

M. Sarfarazi, 2017 .

Genome Scan of Two Large Families with Adult-Onset Primary Open Angle Glaucoma (POAG) Suggests a Probable Locus on 5q33-q35

G. Spaeth, O. Lehmann, A. Child, 2003 .

Family pedigree analysis of children with severe breath-holding spells.

M. Sarfarazi, F. DiMario, 1997, The Journal of pediatrics.

Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.

P. Harper, M. Upadhyaya, M. Sarfarazi, 1987, Journal of medical genetics.

An exclusion map for Von Recklinghausen neurofibromatosis.

J. Edwards, S. Huson, M. Sarfarazi, 1987, Journal of medical genetics.

The use of flanking markers in prediction for Duchenne muscular dystrophy.

P. Harper, M. Sarfarazi, N. Thomas, 1986, Archives of disease in childhood.

A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.

M. Sarfarazi, H. Williams, 1986, Journal of medical genetics.

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis

R. Newcombe, H. Kingston, M. Sarfarazi, 1985, Clinical genetics.

A new locus (GLC1H) for adult-onset primary open-angle glaucoma maps to the 2p15-p16 region.

A. Child, G. Brice, R. Crick, 2007, Archives of ophthalmology.

DNA Probes

P. Harper, M. Upadhyaya, M. Sarfarazi, 2020, Definitions.

Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family

H. Najmabadi, T. Rezaie, M. Sarfarazi, 2007, Ophthalmic genetics.

Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with Waardenburg syndrome Type I

M. Sarfarazi, Vihra N. Sotirova, Tayebeh Rezaie, 2000, Ophthalmic Genetics.

CONGENITAL BLINDNESS:REPORT OF LEBER CONGENITAL AMAUROSISIN A LARGE IRANIAN KINDRED

M. Sarfarazi, T. Rezaei, S. Sohbati, 2001 .

Genetic linkage between the loci for myotonic dystrophy and peptidase D

P. Harper, M. Sarfarazi, T. O'brien, 1983, Annals of human genetics.

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

K. Burnand, S. Mansour, A. Child, 2002, Journal of medical genetics.

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

J. Allanson, P. Harper, M. Upadhyaya, 1991, Journal of medical genetics.

Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.

D. Shaw, P. Harper, M. Sarfarazi, 1986, Journal of medical genetics.

Report on genetic linkage analysis between Huntington's disease and the G8 DNA polymorphism

M. Sarfarazi, 1986, Genetic epidemiology. Supplement.