The genetic significance of accessory bisatellited marker chromosomes

The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype

1981 • 204 citations

A chromosome survey of 2,400 normal newborn infants

1969 • 115 citations

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1977 • 114 citations

Cytogenetic and clinical studies in five cases of inv dup(15)

1979 • 112 citations

Prader‐Willi syndrome and a bisatellited derivative of chromosome 15

1980 • 65 citations

Chromosome survey of a hospital for the mentally subnormal Part 2: Autosome abnormalities

1972 • 60 citations

Chromosome survey of total population of mentally subnormal in North-East of Scotland.

1976 • 55 citations

An aberrant small acrocentric chromosome

1962 • 51 citations

Chromosome findings in 700 children referred to a psychiatric clinic

1972 • 42 citations

Bisatellited extra small metacentric chromosome in newborns

1974 • 40 citations

A Familial Centric Chromosome Fragment

1965 • 39 citations

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

1981 • 38 citations

Seasonal variation in the birth of children with aneuploid chromosome abnormalities

1973 • 37 citations

C‐bands in seven cases of accessory small chromosomes

1977 • 33 citations

Cytogenetic survey of a hospital for the mentally retarded

1976 • 32 citations

Prader‐Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

1979 • 28 citations

Two kinships with accessory bisatellited chromosomes.

1973 • 28 citations

A chromosome survey of a hospital for the mentally subnormal

1979 • 27 citations

Normal phenotype and partial trisomy for the G positive region of chromosome 21.

1979 • 26 citations

A case report of a presumptive +i(18p) associated with serum IgA deficiency

1977 • 26 citations

Significance of detection of extra metacentric microchromosome in amniotic cell culture.

1978 • 25 citations

Small metacentric nonsatellited extra chromosome

1978 • 25 citations

Extra marker chromosome in newborn children

2009 • 23 citations

A familial minute isochromosome.

1966 • 21 citations

Familial extra centric bisatellited chromosome

1969 • 20 citations

Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom

1976 • 20 citations

Genetic studies on a minute centric fragment transmitted through three generations

1970 • 19 citations

Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome.

1975 • 19 citations

Further delineation of the supernumerary chromosome in the Cat‐Eye Syndrome

1977 • 18 citations

Recurrence of Down syndrome associated with microchromosome

1979 • 17 citations

Familial partial trisomy 15.

1977 • 17 citations

Report of five unrelated patients with a small, metacentric, extra chromosome or fragment.

1971 • 17 citations

Extra small metacentric chromosome identified as i(18p).

1979 • 16 citations

Ineffectivity of accessory bisatellited marker chromosomes in inducing meiotic nondisjunction

1983 • 15 citations

An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome.

1970 • 14 citations

RESULTS OF 538 CHROMOSOME STUDIES ON PATIENTS REFERRED FOR CYTOGENETIC ANALYSIS

1972 • 14 citations

Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women.

1970 • 13 citations

Chromosome studies on male patients at a mental subnormality hospital

1971 • 13 citations

Small marker chromosome mosaicism confirmed in two cases ascertained prenatally

1978 • 13 citations

Possible Autosomal Isochromosome in a Malformed Child

1966 • 13 citations

Supernumerary small ring chromosome

1974 • 13 citations

Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture

1979 • 12 citations

Possible origin of a small bisatellited additional chromosome

1980 • 12 citations

Hazards of amniocentesis: An unidentifiable fragment

1978 • 11 citations

Father and daughter with presumptive isochromosome satellites-short arms D or G

1973 • 11 citations

The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibship

1978 • 10 citations

Properties and significance of a small marker chromosome in amniotic fluid cells

1980 • 10 citations

Malformation syndrome associated with small extra chromosome

1980 • 9 citations

The ring nature of a tiny supernumerary chromosome fragment

1980 • 9 citations

[Transmission of a small supernumerary chromosome in a family with two cases of 21 trisomy].

1968 • 9 citations

A masculinizing syndrome associated with a doubly-satellited extra chromosome.

1965 • 8 citations

A 13-year-old girl with karyotype 47,XX,+i(22)(qll)

1981 • 8 citations

Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding robertsonian translocations

1980 • 7 citations

Nucleolus-organiser regions in familial extra metacentric human chromosomes

1980 • 7 citations

A familial bisatellited extra metacentric microchromosome in man

1979 • 6 citations

A Familial Extra Small Marker Autosome in Persons with Normal Phenotype

1979 • 6 citations

[Trisomy 21 by translocation (21q,21q) in two sibs of a mother with a supernumerary microchromosome (author's transl)].

1981 • 5 citations

Familial additional chromosomal fragment ascertained in amniotic cell culture

1981 • 5 citations

Prenatal diagnosis in the presence of an extra small chromosome in amniotic cell culture.

1980 • 4 citations

A comment on the paper: Recurrence of down syndrome associated with microchromosome by C. Ramos, L. Rivera, J. Benitez, E. Tejedor, and A. Sanchez-Cascos

1980 • 4 citations

An inherited 1;G translocation.

1971 • 4 citations