SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME

被引：0

作者：

BARLETTA, C ^{[1
]}

RAGUSA, RM ^{[1
]}

GAROFALO, G ^{[1
]}

SCILLATO, F ^{[1
]}

RUGGERI, M ^{[1
]}

机构：

[1] RAGGIO ITALGENE,I-00040 POMEZIA,ITALY

来源：

ANNALES DE GENETIQUE | 1991年 / 34卷 / 02期

关键词：

FRAGILE SITES; CHROMOSOME-9; CHROMOSOME-10; CHROMOSOME-12; CHROMOSOME-X; CULTURE CONDITIONS;

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Fragile sites on chromosomes 9, at 9p21, 10, at 10q25 and 12, at 12q24, were found in the lymphocytes of some members of three families during the study for detection of a fragile X chromosome. The sites were found to be heritable and folato-sensitive. The genetic implications of these results are discussed.

引用

页码：111 / 114

页数：4

共 12 条

[1] Chromosome fragile sites
Durkin, Sandra G.
Glover, Thomas W.
ANNUAL REVIEW OF GENETICS, 2007, 41 : 169 - 192
[2] Autosomal folate sensitive fragile sites in an autistic Basque sample
Arrieta, I
Nunez, T
Gil, A
Flores, P
Usobiaga, E
Martinez, B
ANNALES DE GENETIQUE, 1996, 39 (02): : 69 - 74
[3] DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME
CARPENTER, NJ
AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (2-3): : 311 - 318
[4] CHROMOSOME EVOLUTION IN THE CERCOPITHECIDAE AND ITS RELATIONSHIP TO HUMAN FRAGILE SITES AND NEOPLASIA
CLEMENTE, IC
PONSA, M
GARCIA, M
EGOZCUE, J
INTERNATIONAL JOURNAL OF PRIMATOLOGY, 1990, 11 (04) : 377 - 398
[5] Fragile sites at the centromere of Chinese hamster chromosomes: a possible mechanism of chromosome loss
Simi, S
Simili, M
Bonatti, S
Campagna, M
Abbondandolo, A
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 397 (02) : 239 - 246
[6] Regulation of fragile sites expression in budding yeast by MEC1, RRM3 and hydroxyurea
Hashash, Nadia
Johnson, Anthony L.
Cha, Rita S.
JOURNAL OF CELL SCIENCE, 2011, 124 (02) : 181 - 185
[7] Identification and analysis of novel microRNAs from fragile sites of human cervical cancer: Computational and experimental approach
Reshmi, G.
Chandra, S. S. Vinod
Babu, V. Janki Mohan
Babu, P. S. Saneesh
Santhi, W. S.
Ramachandran, Surya
Lakshmi, S.
Nair, Achuthsankar S.
Pillai, M. Radhakrishna
GENOMICS, 2011, 97 (06) : 333 - 340
[8] Chromosome Breakage in Human Preimplantation Embryos from Carriers of Structural Chromosomal Abnormalities in Relation to Fragile Sites, Maternal Age, and Poor Sperm Factors
Xanthopoulou, L.
Ghevaria, H.
Mantzouratou, A.
Serhal, P.
Doshi, A.
Delhanty, J. D. A.
CYTOGENETIC AND GENOME RESEARCH, 2012, 136 (01) : 21 - 29
[9] LINKAGE ANALYSIS IN THE FRAGILE-X SYNDROME USING MULTIPLE DISTAL XQ POLYMORPHIC DNA MARKERS
GLASS, IA
PIRRIT, LA
WHITE, EM
BELL, MV
DAVIES, KE
COCKBURN, F
CONNOR, JM
AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (2-3): : 298 - 304
[10] Low-copy repeats on chromosome 22q11.2 show replication timing switches, DNA flexibility peaks and stress inducible asynchrony, sharing instability features with fragile sites
Puliti, Aldamaria
Rizzato, Cosmeri
Conti, Valerio
Bedini, Andrea
Gimelli, Giorgio
Barale, Roberto
Sbrana, Isabella
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2010, 686 (1-2) : 74 - 83

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