A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter Mordechai Shohat, Rona Lotan, Nurit Magal, Tamar.

Slides:

Advertisements

Similar presentations

Connexin Mutations in Skin Disease and Hearing Loss David P. Kelsell, Wei-Li Di, Mark J. Houseman The American Journal of Human Genetics Volume 68, Issue.

Advertisements

Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease- Causing Point Mutations Renee P. Stokowski, David R. Cox The American.

Gene Preference in Maple Syrup Urine Disease Mary M. Nellis, Dean J. Danner The American Journal of Human Genetics Volume 68, Issue 1, Pages (January.

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part I: Methods and Power Analysis Douglas F. Levinson, Matthew D. Levinson, Ricardo Segurado,

Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery Herbert A. Lubs, Roger E. Stevenson, Charles E. Schwartz The American Journal.

Measurement of Relative Copy Number of CDKN2A/ARF and CDKN2B in Bladder Cancer by Real-Time Quantitative PCR and Multiplex Ligation-Dependent Probe Amplification.

The Duty to Recontact: Attitudes of Genetics Service Providers Jennifer L. Fitzpatrick, Cecil Hahn, Teresa Costa, Marlene J. Huggins The American Journal.

Peopling of Sahul: mtDNA Variation in Aboriginal Australian and Papua New Guinean Populations Alan J. Redd, Mark Stoneking The American Journal of Human.

The Trimmed-Haplotype Test for Linkage Disequilibrium

A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3 Giuseppe De Michele, Maurizio De Fusco, Francesca Cavalcanti,

The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23

Transmission/Disequilibrium Tests for Extended Marker Haplotypes

M. A. Escamilla, M. C. DeMille, E. Benavides, E. Roche, L. Almasy, S

Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity Kathrin Saar, Lihadh.

Mapping of Autosomal Dominant Osteopetrosis Type II (Albers-Schönberg Disease) to Chromosome 16p13.3 Olivier Bénichou, Erna Cleiren, Jeppe Gram, Jens.

Schizophrenia and Affective Disorders—Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and.

Genetic Linkage of Paget Disease of the Bone to Chromosome 18q

Robustness and Power of the Maximum-Likelihood–Binomial and Maximum-Likelihood– Score Methods, in Multipoint Linkage Analysis of Affected-Sibship Data

Genetic Linkage Analysis of a Dichotomous Trait Incorporating a Tightly Linked Quantitative Trait in Affected Sib Pairs Jian Huang, Yanming Jiang The.

C. M. van Duijn, M. C. J. Dekker, V. Bonifati, R. J. Galjaard, J. J

Practice Notes from the AAAI

An Autosomal Dominant Thrombocytopenia Gene Maps to Chromosomal Region 10p Anna Savoia, Maria Del Vecchio, Antonio Totaro, Silverio Perrotta, Giovanni.

Meta-analysis of Genetic-Linkage Analysis of Quantitative-Trait Loci

L. M. Downey, T. J. Keen, E. Roberts, D. C. Mansfield, M. Bamashmus, C

Ren-Hua Chung, Richard W. Morris, Li Zhang, Yi-Ju Li, Eden R. Martin

Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland

A Combined Linkage-Physical Map of the Human Genome

The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23

The Novel Genetic Disorder Microhydranencephaly Maps to Chromosome 16p

Genetics, Individuality, and Medicine in the 21st Century*

Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations C. Bourgain, E. Génin, P. Holopainen, K.

The Gene for Severe Combined Immunodeficiency Disease in Athabascan-Speaking Native Americans Is Located on Chromosome 10p Lanying Li, Dennis Drayna,

The American Journal of Human Genetics

Recurrent Williams-Beuren Syndrome in a Sibship Suggestive of Maternal Germ-Line Mosaicism Ali Kara-Mostefa, Odile Raoul, Stanislas Lyonnet, Jeanne Amiel,

Multiplex Bead Suspension Array for Screening Neisseria gonorrhoeae Antibiotic Resistance Genetic Determinants in Noncultured Clinical Samples Sergey.

A Second Gene for Autosomal Dominant Möbius Syndrome Is Localized to Chromosome 10q, in a Dutch Family H.T.F.M. Verzijl, B. van den Helm, B. Veldman,

Identification of a Genetic Locus for Ichthyosis Vulgaris on Chromosome 10q22.3– q24.2 Ping Liu, Qingyu Yang, Xu Wang, Aiping Feng, Tao Yang, Rong Yang,

Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel Hagit Toledano-Alhadef, Lina Basel-Vanagaite, Nurit.

Howard B. Yeon, Noralane M. Lindor, J.G. Seidman, Christine E. Seidman

Tristan F. W. McMullan, Andrew R. Collins, Anthony G. Tyers, David O

Familial Juvenile Hyperuricemic Nephropathy: Localization of the Gene on Chromosome 16p11.2—and Evidence for Genetic Heterogeneity Blanka Stibůrková,

Candidate Locus for a Nuclear Modifier Gene for Maternally Inherited Deafness Yelena Bykhovskaya, Xavier Estivill, Kent Taylor, Tieu Hang, Melanie Hamon,

The Gene for Naegeli–Franceschetti–Jadassohn Syndrome Maps to 17q21

A Locus for Hereditary Sensory Neuropathy with Cough and Gastroesophageal Reflux on Chromosome 3p22-p24 C. Kok, M.L. Kennerson, P.J. Spring, A.J. Ing,

News & Notes Journal of Allergy and Clinical Immunology

Hal M. Hoffman, Fred A. Wright, David H. Broide, Alan A

A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24 S.J. Mitchell, D.P. McHale, D.A. Campbell,

Family-Based Tests of Association in the Presence of Linkage

Erratum The American Journal of Human Genetics

Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

On a Randomization Procedure in Linkage Analysis

John A. Martignetti, Karen E

Long Homozygous Chromosomal Segments in Reference Families from the Centre d'Étude du Polymorphisme Humain Karl W. Broman, James L. Weber The American.

Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11.

Linkage Analysis in a Large Brazilian Family with van der Woude Syndrome Suggests the Existence of a Susceptibility Locus for Cleft Palate at 17p

Genomewide Search and Genetic Localization of a Second Gene Associated with Autosomal Dominant Branchio-Oto-Renal Syndrome: Clinical and Genetic Implications

Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23

Identification, by Homozygosity Mapping, of a Novel Locus for Autosomal Recessive Congenital Ichthyosis on Chromosome 17p, and Evidence for Further Genetic.

A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23 Young-Ae Lee, Howard P.

Kazuhito Sugimura, Kent D

Alice S. Whittemore, Jerry Halpern

Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity Kathrin Saar, Lihadh.

Genetic Linkage Analysis of a Dichotomous Trait Incorporating a Tightly Linked Quantitative Trait in Affected Sib Pairs Jian Huang, Yanming Jiang The.

Sanjay Shete, Xiaojun Zhou, Christopher I. Amos

Zuoheng Wang, Mary Sara McPeek The American Journal of Human Genetics

A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13 I.A. Meijer, C.K. Hand, K.K. Grewal, M.G. Stefanelli, E.J. Ives,

Gonçalo R. Abecasis, Janis E. Wigginton

B. Yuan, R. Neuman, S. H. Duan, J. L. Weber, P. Y. Kwok, N. L

Autosomal Recessive Cerebellar Ataxia with Oculomotor Apraxia (Ataxia- Telangiectasia–Like Syndrome) Is Linked to Chromosome 9q34 Andrea H. Németh, Elena.

Genetic Analysis of Families with Parkinson Disease that Carry the Ala53Thr Mutation in the Gene Encoding α-Synuclein Aglaia Athanassiadou, Gerassimos.

Presentation transcript:

A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter Mordechai Shohat, Rona Lotan, Nurit Magal, Tamar Shohat, Nathan Fischel-Ghodsian, Jerome I. Rotter, Lutfi Jaber The American Journal of Human Genetics Volume 61, Issue 5, Pages 1139-1143 (November 1997) DOI: 10.1086/301598 Copyright © 1997 The American Society of Human Genetics Terms and Conditions

Figure 1 Haplotype of seven markers studied in Israeli-Arab sibships with AMC neuropathic type. The order and distance between the markers are depicted. The American Journal of Human Genetics 1997 61, 1139-1143DOI: (10.1086/301598) Copyright © 1997 The American Society of Human Genetics Terms and Conditions

Figure 2 Typical clinical findings in affected members of family with AMC neuropathic type. The American Journal of Human Genetics 1997 61, 1139-1143DOI: (10.1086/301598) Copyright © 1997 The American Society of Human Genetics Terms and Conditions