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Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation

Data up to Jan 2025

Published1996
Citations77
References23

Total Citations Per Year

Abstract

References (23)

A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES

1971 • 5,049 citations

The Cytogenetics of Mammalian Autosomal Rearrangements

1989 • 393 citations

Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A

1978 • 277 citations

Forty four probands with an additional ?marker? chromosome

1985 • 235 citations

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome

1989 • 164 citations

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis

1992 • 160 citations

Clinical and Molecular Analysis of Five(Inv) Dup(15) Patients

1993 • 136 citations

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

1994 • 128 citations

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.

1993 • 127 citations

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

1979 • 112 citations

Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.

1994 • 107 citations

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

1984 • 98 citations

Inv dup(15) supernumerary marker chromosomes.

1994 • 84 citations

Dinucleotide repeat polymorphism at the GABAA receptor β3 (GABRB3) locus in the Angelman/Prader— Willi region (AS/PWS) of chromosome 15

1992 • 76 citations

Preferential maternal derivation in inv dup(15)

1981 • 71 citations

Prader‐Willi syndrome and a bisatellited derivative of chromosome 15

1980 • 65 citations

Mutation Analysis Provides Additional Proof That Mottled is the Mouse Homologue of Menkes' Disease

1997 • 60 citations

Report of the fourth international workshop on human chromosome 15 mapping 1997

1999 • 56 citations

Report of the, Second International Workshop on Human Chromosome 15 Mapping 1994

1994 • 40 citations

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

1981 • 38 citations

Identification of a marker chromosome as inv dup(15) by molecular analysis

1991 • 17 citations

Autism associated with tetrasomy 15: A further report

1993 • 10 citations

Region-specific cosmids and STRPs identified by chromosome microdissection and fish

1995 • 4 citations

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Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients… (1996) – American Journal of Medical Genetics | Metascience Observatory Explorer