Partial monosomy 8p with minimal dysmorphic signs.

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Am J Med Genet A (2009) 1.40

Distal 8p deletion (8p23.1----8pter): a common deletion? J Med Genet (1992) 1.23

Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome. Am J Hum Genet (2000) 0.96

A case of partial trisomy of chromosome 8p associated with autism. J Autism Dev Disord (2006) 0.91

Partial trisomy 1(q42-->qter): a new case with a mild phenotype. J Med Genet (1998) 0.87

Familial partial trisomy 8p without dysmorphic features and only mild mental retardation. J Med Genet (1995) 0.83

Small structural changes of chromosome 8. Two cases with evidence for deletion. Hum Genet (1977) 1.28

A new chromosome deletion syndrome. Report of a patient with a 46,XY,8p- chromosome constitution. Clin Genet (1976) 1.02

New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome. Eur J Pediatr (1977) 0.97

[Partial deletion of the short arm of chromosome 8]. Ann Genet (1975) 0.97

A case of deletion of short arm of chromosome 8. Birth Defects Orig Artic Ser (1977) 0.93

The 8p- syndrome. Hum Genet (1979) 0.92

4th International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, 5, 7, 8, 10, 11, and 12. Cytogenet Cell Genet (1978) 0.91

[Partial deletion of the short arm of chromosome 8]. Ann Genet (1977) 0.91

The 8p-syndrome. Ann Genet (1989) 0.90

Monosomy 8p: an easily overlooked syndrome. J Med Genet (1986) 0.86

Partial 8p- syndrome. J Genet Hum (1980) 0.85

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. Am J Hum Genet (1999) 1.56

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization. Prenat Diagn (1994) 1.06

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH). Am J Hum Genet (1993) 1.04

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere. Hum Genet (1991) 0.85

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

Interferon system defects in malignant T-cells. Leukemia (1994) 0.79

Deletion of alpha-, beta-, and omega-interferon genes in malignant cells from children with acute lymphocytic leukemia. Cancer Res (1990) 0.79

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

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

Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84. Clin Genet (1991) 0.78

Middle-aged women with Turner's syndrome. Medical status, hormonal treatment and social life. Acta Endocrinol (Copenh) (1991) 0.78

Interferon system in primary acute lymphocytic leukemia cells with or without deletions of the alpha-/beta-interferon genes. Blood (1992) 0.77

[Increasing number of hemoglobinopathies. Rapid diagnosis with DNA technique]. Lakartidningen (1992) 0.75

Acute myelomonocytic leukemia (M4) and t(15;17)(q24;q21). A diagnostic dilemma. Cancer Genet Cytogenet (1993) 0.75

Deletion of chromosome 2(p13) is a nonrandomly occurring karyotypic abnormality in myelodysplastic syndrome. Cancer Genet Cytogenet (1992) 0.75

Length polymorphism of heterochromatic segment of the Y chromosome in boys with acute leukemia. Acta Paediatr Jpn (1995) 0.75

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

[Diagnosis of cystic fibrosis by means of genetic technology--guidelines from an expert meeting]. Lakartidningen (1990) 0.75