Access the full text.
Sign up today, get DeepDyve free for 14 days.
G Stetten, B Sroka‐Zaczek, V Corson (1981)
Prenatal detection of an accessory chromosome identified as an inversion duplication (15), 57
J. Hamerton, N. Canning, M. Ray, Shelley Smith (1975)
A cytogenetic survey of 14,069 newborn infantsClinical Genetics, 8
A. Daniel, P. Malafiej, K. Preece, N. Chia, J. Nelson, M. Smith (1994)
Identification of marker chromosomes in thirteen patients using FISH probing.American journal of medical genetics, 53 1
J Müller‐Navia, A Nebel, E Schleiermacher (1995)
Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis, 96
DM Cox, CM Bradley, A Robinson (1981)
A non‐robertsonian t(21;21) translocation in a patient with Down's syndrome associated with familial supernumerary bisatellited small marker chromosome, 33
D. Warburton (1991)
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.American journal of human genetics, 49 5
P. Meltzer, X. Guan, A. Burgess, J. Trent (1992)
Rapid generation of region specific probes by chromosome microdissection and their applicationNature Genetics, 1
R. Viersbach, H. Engels, G. Schwanitz (1997)
Identification of supernumerary der(20) chromosomes by FISH in three patients.American journal of medical genetics, 70 3
N. Carter, M. Ferguson-Smith, M. Perryman, H. Telenius, A. Pelmear, M. Leversha, M. Glancy, S. Wood, K. Cook, H. Dyson, M. Ferguson-Smith, L. Willatt (1992)
Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.Journal of Medical Genetics, 29
H. Telenius, N. Carter, C. Bebb, Magnus Nordenskjo¨ld, B. Ponder, A. Tunnacliffe (1992)
Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.Genomics, 13 3
R. Schubert, R. Viersbach, Thomas Eggermann, M. Hansmann, G. Schwanitz (1997)
Report of two new cases of Pallister-Killian syndrome confirmed by FISH: tissue-specific mosaicism and loss of i(12p) by in vitro selection.American journal of medical genetics, 72 1
D. Pinkel, T. Straume, J. Gray (1986)
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.Proceedings of the National Academy of Sciences of the United States of America, 83 9
P. Jacobs, M. Melville, S. Ratcliffe, A. Keay, J. Syme (1974)
A cytogenetic survey of 11,680 newborn infantsAnnals of Human Genetics, 37
C. Gravholt, U. Friedrich (1995)
Quantitative comparison of FMR1 gene expression in normal and premutation alleles.American Journal of Medical Genetics, 56
D. Callen, H. Eyre, Yip My, J. Freemantle, E. Haan (1992)
Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.American journal of medical genetics, 43 4
E. Blennow, K. Nielsen, H. Telenius, N. Carter, U. Kristoffersson, E. Holmberg, C. Gillberg, M. Nordenskjöld (1995)
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.American journal of medical genetics, 55 1
E. Sachs, J. Hemel, J. Hollander, M. Jahoda (1987)
Marker chromosomes in A series of 10000 prenatal diagnoses. Cytogenetic and follow‐up studiesPrenatal Diagnosis, 7
J Nielsen, M Wohlert (1991)
Chromosome abnormalities found among 34,910 newborn children: Results from a 13‐year incidence study in Århus, Denmark, 87
E. Blennow, T. Bui, U. Kristoffersson, M. Vujić, G. Annéren, E. Holmberg, M. Nordenskjöld (1994)
Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridizationPrenatal Diagnosis, 14
M. Urioste, G. Visedo, A. Sanchis, C. Sentís, A. Villa, P. Ludeña, J. Hortigüela, M. Martínez‐Frías, J. Fernández-Piqueras (1994)
Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.American journal of medical genetics, 49 1
H Fujita, Y Sakamoto, Y Hamamoto (1980)
An extra idic(15p)(q11) chromosome in Prader‐Willi syndrome, 55
C Højbjerg Gravholt, U Friedrich (1995)
Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children, 56
G. Annéren, J. Wahlström, N. Tommerup (1984)
Marker chromosomes in parents to children with Down's syndromeClinical Genetics, 25
N. Spinner, E. Zackai, Sou-De Cheng, J. Knoll (1995)
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.American journal of medical genetics, 57 1
J. Nielsen, K. Rasmussen (2009)
Extra marker chromosome in newborn children.Hereditas, 81 2
D. Callen, H. Eyre, G. Dolman, M. Garry-Battersby, J. McCreanor, A. Valeba, J. Mcgill (1995)
Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.Journal of Medical Genetics, 32
G. Bargman, R. Neu, H. Powers, L. Gardner (1970)
48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome.Journal of Medical Genetics, 7
D. Ledbetter, J. Mascarello, V. Riccardi, V. Harper, S. Airhart, R. Strobel (1982)
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.American journal of human genetics, 34 2
B. Migeon, Shengyuan Luo, M. Jani, Peter Jeppesen (1994)
The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.American journal of human genetics, 55 3
JL Hamerton, N Canning, M Ray, S Smith (1975)
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities, 8
C Ramos, L Rivera, J Benitez, E Tejedor, A Sanchez‐Cascos (1979)
Recurrence of Down syndrome associated with microchromosome, 49
E. Wulfsberg, R. Sparkes, I. Klisak, W. Gurfield, J. Opitz (1982)
A 15 → 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)American Journal of Medical Genetics, 13
J. Crolla, N. Dennis, P. Jacobs (1992)
A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.Journal of Medical Genetics, 29
Colin Collins, W. Kuo, R. Segraves, J. Fuscoe, D. Pinkel, J. Gray (1991)
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes.Genomics, 11 4
M. Thangavelu, E. Pergament, Rafael Iii, S. Bohlander (1994)
Characterization of marker chromosomes by microdissection and fluorescence in situ hybridizationPrenatal Diagnosis, 14
L. Wisniewski, M. Witt, F. Ginsberg‐Fellner, Judith Wilner, R. Desnick (1980)
Prader‐Willi syndrome and a bisatellited derivative of chromosome 15Clinical Genetics, 18
KE Buckton, G Spowart, MS Newton, H‐J Evans (1985)
Forty four probands with an additional “marker” chromosome, 69
Wendy Robinson, Joseph Wagstaff, F. Bernasconi, Carlo Baccichetti, Lina, Artifoni, Emilio Franzoni, Lorraine Suslak, L. Shih, Hannah Aviv, A. Schinzel (1993)
Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.Journal of Medical Genetics, 30
R. James, I. Temple, N. Dennis, J. Crolla (1995)
A Search for Uniparental Disomy in Carriers of Supernumerary Marker ChromosomesEuropean Journal of Human Genetics, 3
G Senger, I Chubdoba, N Rubsov, U Claussen (1997)
Identifizierung strukturell veränderter Chromosomen durch Mikrosezierung und “reverse painting.”, 9
D. Wolff, Carolyn Brown, Stuart Schwartz, Alessandra Duncan, U. Surti, H. Willard (1994)
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.American journal of human genetics, 55 1
R Viersbach, G Schwanitz, MM Nöthen (1994)
Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP‐PCR amplified microdissected chromosomes, 93
We present cytogenetic and clinical data on 38 patients with supernumerary marker chromosomes (SMCs). SMCs were characterized using a strategy combining classical banding techniques and molecular cytogenetic studies. Cases were ascertained prenatally, postnatally, and after fetal death.
American Journal of Medical Genetics Part A – Wiley
Published: Jan 1, 1998
Keywords: ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.