Brancolini V - Search Results

1

Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p.

Vitale E, Brancolini V, De Rienzo A, Bird L, Allada V, Sklansky M, Chae CU, Ferrero GB, Weber J, Devoto M, Casey B. Vitale E, et al. Among authors: brancolini v. J Med Genet. 2001 Mar;38(3):182-5. doi: 10.1136/jmg.38.3.182. J Med Genet. 2001. PMID: 11303511 Free PMC article. No abstract available.

2

Exclusion of linkage between RET and neuronal intestinal dysplasia type B.

Barone V, Weber D, Luo Y, Brancolini V, Devoto M, Romeo G. Barone V, et al. Among authors: brancolini v. Am J Med Genet. 1996 Mar 15;62(2):195-8. doi: 10.1002/(SICI)1096-8628(19960315)62:2<195::AID-AJMG15>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8882403

3

Genetic linkage studies for the identification of cancer-related genes.

Brancolini V, Devoto M. Brancolini V, et al. Ann Ist Super Sanita. 1996;32(1):173-80. Ann Ist Super Sanita. 1996. PMID: 8967721 Review.

4

The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28.

Auricchio A, Brancolini V, Casari G, Milla PJ, Smith VV, Devoto M, Ballabio A. Auricchio A, et al. Among authors: brancolini v. Am J Hum Genet. 1996 Apr;58(4):743-8. Am J Hum Genet. 1996. PMID: 8644737 Free PMC article.

5

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing.

Bolino A, Brancolini V, Bono F, Bruni A, Gambardella A, Romeo G, Quattrone A, Devoto M. Bolino A, et al. Among authors: brancolini v. Hum Mol Genet. 1996 Jul;5(7):1051-4. doi: 10.1093/hmg/5.7.1051. Hum Mol Genet. 1996. PMID: 8817346

6

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease.

Andrew LJ, Brancolini V, de la Pena LS, Devoto M, Caeiro F, Marchegiani R, Reginato A, Gaucher A, Netter P, Gillet P, Loeuille D, Prockop DJ, Carr A, Wordsworth BF, Lathrop M, Butcher S, Considine E, Everts K, Nicod A, Walsh S, Williams CJ. Andrew LJ, et al. Among authors: brancolini v. Am J Hum Genet. 1999 Jan;64(1):136-45. doi: 10.1086/302186. Am J Hum Genet. 1999. PMID: 9915952 Free PMC article.

7

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

Gambardella A, Bolino A, Muglia M, Valentino P, Bono F, Oliveri RL, Sabatelli M, Brancolini V, Van Broeckhoven C, Romeo G, Devoto M, Quattrone A. Gambardella A, et al. Among authors: brancolini v. Neurology. 1998 Mar;50(3):799-801. doi: 10.1212/wnl.50.3.799. Neurology. 1998. PMID: 9521281

8

[Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage].

Arcos-Burgos M, Palacio LG, Jiménez I, Pineda N, Mora O, Sánchez JL, Jiménez M, Muñoz A, Brancolini V, Devoto M, Ruiz-Linares A. Arcos-Burgos M, et al. Among authors: brancolini v. Rev Neurol. 1998 Jan;26(149):50-2. Rev Neurol. 1998. PMID: 9580275 Spanish.

9

Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct founders.

Bleasel JF, Holderbaum D, Brancolini V, Moskowitz RW, Considine EL, Prockop DJ, Devoto M, Williams CJ. Bleasel JF, et al. Among authors: brancolini v. Hum Mutat. 1998;12(3):172-6. doi: 10.1002/(SICI)1098-1004(1998)12:3<172::AID-HUMU4>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9711874

10

Arg519-Cys mutation in COL2A1: evidence for multiple founders.

Bleasel JF, Holderbaum D, Brancolini V, Moskowitz RW, Haqqi TM, Considine E, Prockop DJ, Devoto M, Williams CJ. Bleasel JF, et al. Among authors: brancolini v. Ann N Y Acad Sci. 1996 Jun 8;785:215-8. doi: 10.1111/j.1749-6632.1996.tb56265.x. Ann N Y Acad Sci. 1996. PMID: 8702133 No abstract available.

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