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Author/Creator Lathrop, M

1. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci. Issue 2 (2nd February 2004)

Authors:
Modamio-Høybjør, S; Moreno-Pelayo, M A; Mencía, A; del Castillo, I; Chardenoux, S; Morais, D; Lathrop, M; Petit, C; Moreno, F
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 2(2004)
Page Start:
e14
Record Type:
Journal Article
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2. DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23. Issue 11 (19th November 2003)

Authors:
Moreno-Pelayo, M A; Modamio-Høybjør, S; Mencía, A; del Castillo, I; Chardenoux, S; Fernández-Burriel, M; Lathrop, M; Petit, C; Moreno, F
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 11(2003)
Page Start:
832
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Genome-wide association meta-analysis in 652, 134 participants identifies 9 novel susceptibility loci for aortic stenosis. (25th November 2020)

Authors:
Chen, H.Y; Small, A.M; Dina, C; Cairns, B.J; Whitmer, R.A; Lathrop, M; Smith, J.G; Holm, H; Wells, Q.S; Rader, D.J; Soderberg, S; Schott, J.J; Engert, J.C; Thanassoulis, G
Journal:
European heart journal
Issue:
Volume 41:(2020)Supplement 2
Page Start:
Record Type:
Journal Article
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4. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. Issue 10 (1st October 2002)

Authors:
Van Maldergem, L; Magré, J; Khallouf, T E; Gedde-Dahl, T; Delépine, M; Trygstad, O; Seemanova, E; Stephenson, T; Albott, C S; Bonnici, F; Panz, V R; Medina, J-L; Bogalho, P; Huet, F; Savasta, S; Verloes, A; Robert, J-J; Loret, H; de Kerdanet, M; Tubiana-Rufi, N
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 10(2002)
Page Start:
722
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease. Issue 3 (2nd March 2005)

Authors:
Pelet, A; de Pontual, L; Clément-Ziza, M; Salomon, R; Mugnier, C; Matsuda, F; Lathrop, M; Munnich, A; Feingold, J; Lyonnet, S; Abel, L; Amiel, J
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 3(2005)
Page Start:
e18
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗