Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 8

1.

FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.

Chu TW, Teebi AS, Gibson L, Breg WR, Yang-Feng TL.

Am J Med Genet. 1994 Aug 1;52(1):92-6.

PMID:
7977471
2.

Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3).

Sparkes RS, Sparkes MC, Kalina RE, Pagon RA, Salk DJ, Disteche CM.

Hum Genet. 1984;68(3):258-9.

PMID:
6500578
3.

Paracentric inversions in man.

Madan K, Seabright M, Lindenbaum RH, Bobrow M.

J Med Genet. 1984 Dec;21(6):407-12. Review.

4.

A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.

Kondo I, Shin K, Honmura S, Nakajima H, Yamamura E, Satoh H, Terauchi M, Usuki Y, Takita H, Hamaguchi H.

Hum Genet. 1985;71(3):263-6.

PMID:
3864729
5.

Familial retinoblastoma (mother and son) with 13q14 deletion.

Fukushima Y, Kuroki Y, Ito T, Kondo I, Nishigaki I.

Hum Genet. 1987 Oct;77(2):104-7.

PMID:
3653883
6.

Deletion (13)(q14.1q14.3) in two generations: variability of ocular manifestations and definition of the phenotype.

Wilson WG, Campochiaro PA, Conway BP, Carter BT, Sudduth KW, Watson BA, Sparkes RS.

Am J Med Genet. 1987 Nov;28(3):675-83. Review.

PMID:
3322010
7.

Constitutional karyotype in retinoblastoma. Case report and review of literature.

Munier F, Pescia G, Jotterand-Bellomo M, Balmer A, Gailloud C, Thonney F.

Ophthalmic Paediatr Genet. 1989 Jun;10(2):129-50. Review.

PMID:
2674826
8.

Retinoblastoma and subband deletion of chromosome 13.

Yunis JJ, Ramsay N.

Am J Dis Child. 1978 Feb;132(2):161-3.

PMID:
626181

Supplemental Content

Support Center