Weissenbach J - Search Results

1

A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.

Bonnet D, Pelet A, Legeai-Mallet L, Sidi D, Mathieu M, Parent P, Plauchu H, Serville F, Schinzel A, Weissenbach J, et al. Bonnet D, et al. Among authors: weissenbach j. Nat Genet. 1994 Apr;6(4):405-8. doi: 10.1038/ng0494-405. Nat Genet. 1994. PMID: 8054983

2

A gene for achondroplasia-hypochondroplasia maps to chromosome 4p.

Le Merrer M, Rousseau F, Legeai-Mallet L, Landais JC, Pelet A, Bonaventure J, Sanak M, Weissenbach J, Stoll C, Munnich A, et al. Le Merrer M, et al. Among authors: weissenbach j. Nat Genet. 1994 Mar;6(3):318-21. doi: 10.1038/ng0394-318. Nat Genet. 1994. PMID: 8012398

3

A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.

Lyonnet S, Bolino A, Pelet A, Abel L, Nihoul-Fékété C, Briard ML, Mok-Siu V, Kaariainen H, Martucciello G, Lerone M, Puliti A, Luo Y, Weissenbach J, Devoto M, Munnich A, Romeo G. Lyonnet S, et al. Among authors: weissenbach j. Nat Genet. 1993 Aug;4(4):346-50. doi: 10.1038/ng0893-346. Nat Genet. 1993. PMID: 8401580

4

[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].

Bonnet D, Terrett J, Pequignot-Viegas E, Weissenbach J, Munnich A, Lyonnet S, Kachaner J. Bonnet D, et al. Among authors: weissenbach j. Arch Mal Coeur Vaiss. 1995 May;88(5):661-6. Arch Mal Coeur Vaiss. 1995. PMID: 7646274 Review. French.

5

An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.

Petit C, Melki J, Levilliers J, Serville F, Weissenbach J, Maroteaux P. Petit C, et al. Among authors: weissenbach j. Hum Genet. 1990 Jul;85(2):247-50. doi: 10.1007/BF00193206. Hum Genet. 1990. PMID: 2370057

6

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

Vincent P, Plauchu H, Hazan J, Fauré S, Weissenbach J, Godet J. Vincent P, et al. Among authors: weissenbach j. Hum Mol Genet. 1995 May;4(5):945-9. doi: 10.1093/hmg/4.5.945. Hum Mol Genet. 1995. PMID: 7633456

7

No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis.

Ma HW, Lajeunie E, Le Merrer M, de Parseval N, Serville F, Weissenbach J, Munnich A, Renier D. Ma HW, et al. Among authors: weissenbach j. Hum Genet. 1995 Dec;96(6):731-5. doi: 10.1007/BF00210308. Hum Genet. 1995. PMID: 8522336

8

Clinical and genetic heterogeneity of hypochondroplasia.

Rousseau F, Bonaventure J, Legeai-Mallet L, Schmidt H, Weissenbach J, Maroteaux P, Munnich A, Le Merrer M. Rousseau F, et al. Among authors: weissenbach j. J Med Genet. 1996 Sep;33(9):749-52. doi: 10.1136/jmg.33.9.749. J Med Genet. 1996. PMID: 8880574 Free PMC article.

9

A gene for familial hemiplegic migraine maps to chromosome 19.

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al. Joutel A, et al. Among authors: weissenbach j. Nat Genet. 1993 Sep;5(1):40-5. doi: 10.1038/ng0993-40. Nat Genet. 1993. PMID: 8220421

10

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.

Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, et al. Tournier-Lasserve E, et al. Among authors: weissenbach j. Nat Genet. 1993 Mar;3(3):256-9. doi: 10.1038/ng0393-256. Nat Genet. 1993. PMID: 8485581

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