| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.
|
Am J Hum Genet
|
1999
|
1.56
|
|
2
|
Partial monosomy 8p with minimal dysmorphic signs.
|
J Med Genet
|
1990
|
0.97
|
|
3
|
Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.
|
Hum Genet
|
1991
|
0.85
|
|
4
|
Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13.
|
Am J Med Genet
|
1992
|
0.83
|
|
5
|
Interferon system defects in malignant T-cells.
|
Leukemia
|
1994
|
0.79
|
|
6
|
Deletion of alpha-, beta-, and omega-interferon genes in malignant cells from children with acute lymphocytic leukemia.
|
Cancer Res
|
1990
|
0.79
|
|
7
|
Middle-aged women with Turner's syndrome. Medical status, hormonal treatment and social life.
|
Acta Endocrinol (Copenh)
|
1991
|
0.78
|
|
8
|
Prenatal investigation of a 45,X/46,X,r(?) karyotype in amniocytes using fluorescence in situ hybridization with an X-centromeric probe.
|
Prenat Diagn
|
1992
|
0.78
|
|
9
|
Deletions of the short arm of chromosome 9, including the interferon-alpha/-beta genes, in acute lymphocytic leukemia. Studies on loss of heterozygosity, parental origin of deleted genes and prognosis.
|
Int J Cancer
|
1993
|
0.78
|
|
10
|
Interferon system in primary acute lymphocytic leukemia cells with or without deletions of the alpha-/beta-interferon genes.
|
Blood
|
1992
|
0.77
|
|
11
|
[Diagnosis of cystic fibrosis by means of genetic technology--guidelines from an expert meeting].
|
Lakartidningen
|
1990
|
0.75
|
|
12
|
Multiple genetic events involving RB1 gene deletion and amplification of chromosome 21 in a case of acute lymphocytic leukemia.
|
Genes Chromosomes Cancer
|
1994
|
0.75
|
|
13
|
Acute myelomonocytic leukemia (M4) and t(15;17)(q24;q21). A diagnostic dilemma.
|
Cancer Genet Cytogenet
|
1993
|
0.75
|
|
14
|
Length polymorphism of heterochromatic segment of the Y chromosome in boys with acute leukemia.
|
Acta Paediatr Jpn
|
1995
|
0.75
|
|
15
|
[Increasing number of hemoglobinopathies. Rapid diagnosis with DNA technique].
|
Lakartidningen
|
1992
|
0.75
|
|
16
|
Deletion of chromosome 2(p13) is a nonrandomly occurring karyotypic abnormality in myelodysplastic syndrome.
|
Cancer Genet Cytogenet
|
1992
|
0.75
|