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Items: 1 to 20 of 22

1.

A girl with duplication 17p10-p12 associated with a dicentric chromosome.

Shaw CJ, Stankiewicz P, Christodoulou J, Smith E, Jones K, Lupski JR.

Am J Med Genet A. 2004 Jan 15;124A(2):173-8.

PMID:
14699617
2.

Segregation analysis in reciprocal translocation carriers.

Petrosky DL, Borgaonkar DS.

Am J Med Genet. 1984 Sep;19(1):137-59.

PMID:
6496566
3.

Silver staining and the 17ps chromosome.

Patil SR, Bent FC.

Clin Genet. 1980 Apr;17(4):281-4.

PMID:
6154552
4.

Significance of chromosome 17ps+ in three generations of a family.

Priest JH, Peakman DC, Patil SR, Robinson A.

J Med Genet. 1970 Jun;7(2):142-7. No abstract available.

5.

Chromosomal heteromorphisms in the assignment of loci to particular autosomes: a study of four pedigrees.

Wikramanayake E, Renwick JH, Ferguson-Smith MA.

Ann Genet. 1971 Dec;14(4):245-56. No abstract available.

PMID:
5316128
6.

[Study of a 46,XX-46,XX,17r mosaicism].

Petit P, Koulischer L.

Ann Genet. 1971 Mar;14(1):55-8. French. No abstract available.

PMID:
5314296
7.

Chromosome findings in 700 children referred to a psychiatric clinic.

Crandall BF, Carrel RE, Sparkes RS.

J Pediatr. 1972 Jan;80(1):62-8. No abstract available.

PMID:
5016354
8.

Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Mikelsaar AV, Tüür SJ, Käosaar ME.

Humangenetik. 1973;20(2):89-101. No abstract available.

PMID:
4785172
9.

Three translocations involving C- or G-group chromosomes.

Nakagome Y, Inuma K, Matsui I.

J Med Genet. 1973 Jun;10(2):174-6. No abstract available.

10.

Chromosome investigation in married couples with repeated spontaneous abortions.

Käosaar ME, Mikelsaar AV.

Humangenetik. 1973;17(4):277-83. No abstract available.

PMID:
4694509
11.

A 17p marker chromosome familial study.

Sandstrom MM, Jenkins EC.

Ann Genet. 1973 Dec;16(4):267-9. No abstract available.

PMID:
4544091
12.

Structural variation in human nitotic chromosomes.

Leisti J.

Ann Acad Sci Fenn Biol. 1971;179:1-69. No abstract available.

PMID:
4261167
13.

[A familial case of 17 r ring-shaped chromosome of group E with transmission from father to son].

Burden M, Lupaşcu E, Mărgineanu L.

Rev Med Chir Soc Med Nat Iasi. 1973 Apr-Jun;77(2):353-7. Romanian. No abstract available.

PMID:
4146973
14.

An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.

Borgaonkar DS, McKusick VA, Farber PA.

J Med Genet. 1973 Dec;10(4):379-84. No abstract available.

15.

Routine application of high resolution chromosome analysis.

Hoo JJ.

Am J Med Genet. 1986 Jul;24(3):533-9. No abstract available.

PMID:
3728572
16.

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly.

Greenberg F, Courtney KB, Wessels RA, Huhta J, Carpenter RJ, Rich DC, Ledbetter DH.

Am J Med Genet. 1988 Sep;31(1):1-4.

PMID:
3066218
17.

VNTR (variable number of tandem repeats) markers show loss of chromosome 17p sequences in human colorectal carcinomas.

Lothe RA, Nakamura Y, Woodward S, Gedde-Dahl T Jr, White R.

Cytogenet Cell Genet. 1988;48(3):167-9.

PMID:
2906851
18.

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.

Baker SJ, Fearon ER, Nigro JM, Hamilton SR, Preisinger AC, Jessup JM, vanTuinen P, Ledbetter DH, Barker DF, Nakamura Y, White R, Vogelstein B.

Science. 1989 Apr 14;244(4901):217-21.

PMID:
2649981
19.

Ring 17 chromosome detected by amniocentesis.

Weinberg AG, Bair JL, Harrod MJ.

Humangenetik. 1975 Jul 23;28(3):269-72.

PMID:
1150287
20.

Chromosome studies in patients with congenital malformations and mental retardation.

Erdtmann B, Salzano FM, Mattevi MS.

Humangenetik. 1975;26(4):297-306.

PMID:
1150230

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