J. P. Lin

发表

Familial autoimmunity in pedigrees of idiopathic inflammatory myopathy patients suggests common genetic risk factors for many autoimmune diseases.

S. Bale, F. Miller, P. Plotz, 1998, Arthritis and rheumatism.

Parental transmission and D18S37 allele sharing in bipolar affective disorder

S. Bale, Jingping Lin, J. P. Lin, 1997, Genetic epidemiology.

Rheumatoid arthritis in the Pima Indians: the intersection of epidemiologic, demographic, and genealogic data.

R. Hirsch, S. Pillemer, D. Bloch, 1998, Arthritis and rheumatism.

Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita.

R. Webster, J. Newsom-Davis, B. Neville, 2001, The Journal of clinical investigation.

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex.

C. Stratakis, J. Carney, L. Kirschner, 2000, Human molecular genetics.

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

D. Papanicolaou, D. Kastner, G. Chrousos, 1996, The Journal of clinical investigation.

Evidence for genetic heterogeneity in monilethrix.

S. Bale, P. Itin, G. Richard, 1996, The Journal of investigative dermatology.

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers.

C. Stratakis, E. Pras, O. Rennert, 1997, Proceedings of the Association of American Physicians.

A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.

E. Jabs, V. Kimonis, D. Gelber, 1999, American journal of human genetics.

Journal of Clinical Endocrinology and Metabolism Printed in U.S.A. Copyright © 1998 by The Endocrine Society Familial Hyperaldosteronism Type II: Description of a Large Kindred and Exclusion of the Aldosterone

G. Chrousos, C. Stratakis, D. Torpy, 2022 .

Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).

C. Stratakis, O. Rennert, J. P. Lin, 1998, American journal of medical genetics.

Linkage studies in erythrokeratodermias: fine mapping, genetic heterogeneity and analysis of candidate genes.

S. Bale, P. Itin, G. Richard, 1997, The Journal of investigative dermatology.