Lerone M - Search Results

1

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

Seri M, Cusano R, Forabosco P, Cinti R, Caroli F, Picco P, Bini R, Morra VB, De Michele G, Lerone M, Silengo M, Pela I, Borrone C, Romeo G, Devoto M. Seri M, et al. Among authors: lerone m. Am J Hum Genet. 1999 Feb;64(2):586-93. doi: 10.1086/302241. Am J Hum Genet. 1999. PMID: 9973297 Free PMC article.

2

Autosomal recessive microcephaly with early onset seizures and spasticity.

Silengo M, Lerone M, Martinelli M, Martucciello G, Caffarena PE, Jasonni V, Romeo G. Silengo M, et al. Among authors: lerone m. Clin Genet. 1992 Sep;42(3):152-5. doi: 10.1111/j.1399-0004.1992.tb03228.x. Clin Genet. 1992. PMID: 1395086

3

Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasia.

Lerone M, Soliani M, Corea D, Romeo G, Martucciello G, Silengo MC. Lerone M, et al. Am J Med Genet. 1992 Dec 1;44(6):827-9. doi: 10.1002/ajmg.1320440623. Am J Med Genet. 1992. PMID: 1481856

4

Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new case.

Lerone M, Pessagno A, Taccone A, Poggi G, Romeo G, Silengo MC. Lerone M, et al. Clin Genet. 1992 Feb;41(2):87-9. doi: 10.1111/j.1399-0004.1992.tb03639.x. Clin Genet. 1992. PMID: 1544218

5

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Archidiacono N, Lerone M, Rocchi M, Anvret M, Ozcelik T, Francke U, Romeo G. Archidiacono N, et al. Among authors: lerone m. Hum Genet. 1991 Apr;86(6):604-6. doi: 10.1007/BF00201549. Hum Genet. 1991. PMID: 1673961

6

Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvement.

Lerone M, Dodero P, Romeo G, Martucciello G, Caffarena PE, Brisigotti M, Toma P, Taccone A, Silengo M. Lerone M, et al. Pediatr Radiol. 1991;21(8):578-9. doi: 10.1007/BF02012602. Pediatr Radiol. 1991. PMID: 1815180

7

Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene.

Covone AE, Lerone M, Romeo G. Covone AE, et al. Among authors: lerone m. Hum Genet. 1991 Jul;87(3):353-60. doi: 10.1007/BF00200919. Hum Genet. 1991. PMID: 1864612

8

[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism].

Covone AE, Caroli F, Cereseto A, Lerone M, Romeo G. Covone AE, et al. Among authors: lerone m. Minerva Pediatr. 1991 Mar;43(3):65-6. Minerva Pediatr. 1991. PMID: 1870527 Italian. No abstract available.

9

Multiple sutural synostosis and congenital cataracts.

Lerone M, Romeo G, Conrad E, Silvano S, Cama A, Silengo CM. Lerone M, et al. Hum Genet. 1991 Oct;87(6):758. doi: 10.1007/BF00201745. Hum Genet. 1991. PMID: 1937484 No abstract available.

10

A new syndrome with cerebro-oculo-skeletal-renal involvement.

Silengo MC, Lerone M, Pelizza A, Gatti R, Barabino A, Romeo G. Silengo MC, et al. Among authors: lerone m. Pediatr Radiol. 1990;20(8):612-4. doi: 10.1007/BF02129073. Pediatr Radiol. 1990. PMID: 2251013

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