Camerino G - Search Results

1

Three DNA markers for hypophosphataemic rickets.

Rowe PS, Read AP, Mountford R, Benham F, Kruse TA, Camerino G, Davies KE, O'Riordan JL. Rowe PS, et al. Among authors: camerino g. Hum Genet. 1992 Jul;89(5):539-42. doi: 10.1007/BF00219180. Hum Genet. 1992. PMID: 1353055

2

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Drayna D, Davies K, Hartley D, Mandel JL, Camerino G, Williamson R, White R. Drayna D, et al. Among authors: camerino g. Proc Natl Acad Sci U S A. 1984 May;81(9):2836-9. doi: 10.1073/pnas.81.9.2836. Proc Natl Acad Sci U S A. 1984. PMID: 6326147 Free PMC article.

3

Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

Oberlé I, Camerino G, Wrogemann K, Arveiler B, Hanauer A, Raimondi E, Mandel JL. Oberlé I, et al. Among authors: camerino g. Hum Genet. 1987 Sep;77(1):60-5. doi: 10.1007/BF00284716. Hum Genet. 1987. PMID: 3502701

4

X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region.

Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA. Mostacciuolo ML, et al. Among authors: camerino g. Hum Genet. 1991 May;87(1):23-7. doi: 10.1007/BF01213086. Hum Genet. 1991. PMID: 1674715

5

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

Bardoni B, Guioli S, Maserati E, Maraschio P, Camerino G. Bardoni B, et al. Among authors: camerino g. Hum Genet. 1988 Dec;81(1):23-5. doi: 10.1007/BF00283723. Hum Genet. 1988. PMID: 2904403

6

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.

Oberlé I, Camerino G, Kloepfer C, Moisan JP, Grzeschik KH, Hellkuhl B, Hors-Cayla MC, Van Cong N, Weil D, Mandel JL. Oberlé I, et al. Among authors: camerino g. Hum Genet. 1986 Jan;72(1):43-9. doi: 10.1007/BF00278816. Hum Genet. 1986. PMID: 3002952

7

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.

Henke A, Wapenaar M, van Ommen GJ, Maraschio P, Camerino G, Rappold G. Henke A, et al. Among authors: camerino g. Am J Hum Genet. 1991 Oct;49(4):811-9. Am J Hum Genet. 1991. PMID: 1897527 Free PMC article.

8

A new MspI restriction fragment length polymorphism in the hemophilia B locus.

Camerino G, Oberlé I, Drayna D, Mandel JL. Camerino G, et al. Hum Genet. 1985;71(1):79-81. doi: 10.1007/BF00295673. Hum Genet. 1985. PMID: 2411652

9

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

Maestrini E, Rivella S, Tribioli C, Rocchi M, Camerino G, Santachiara-Benerecetti S, Parolini O, Notarangelo LD, Toniolo D. Maestrini E, et al. Among authors: camerino g. Am J Hum Genet. 1992 Jan;50(1):156-63. Am J Hum Genet. 1992. PMID: 1346076 Free PMC article.

10

Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23.

Caiulo A, Nicolis S, Bianchi P, Zuffardi O, Bardoni B, Maraschio P, Ottolenghi S, Camerino G, Giglioni B. Caiulo A, et al. Among authors: camerino g. Hum Genet. 1991 Feb;86(4):388-90. doi: 10.1007/BF00201840. Hum Genet. 1991. PMID: 1999341

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