DOI: 10.1086/301932. A Severely Affected Male Born into a Rett Syndrome Kindred Supports X-Linked Inheritance and Allows Extension of the Exclusion Map

A Severely Affected Male Born into a Rett Syndrome Kindred Supports X-Linked Inheritance and Allows Extension of the Exclusion Map

10.1086/301932

Crossref journal-article

Elsevier BV

The American Journal of Human Genetics (78)

Bibliography

Schanen, C., & Francke, U. (1998). A Severely Affected Male Born into a Rett Syndrome Kindred Supports X-Linked Inheritance and Allows Extension of the Exclusion Map. The American Journal of Human Genetics, 63(1), 267â269.

Authors 2

Carolyn Schanen (first)
Uta Francke (additional)

References 9 Referenced 74

10.1007/BF00201549 / Hum Genet / Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations by Archidiacono (1991)
{'key': '10.1086/301932_bib2', 'series-title': 'Hoping for the impossible', 'author': 'Brown', 'year': '1997'} / Hoping for the impossible by Brown (1997)
10.1038/380152a0 / Nature / A comprehensive genetic map of the human genome based on 5,264 microsatellites by Dib (1996)
{'key': '10.1086/301932_bib4', 'first-page': '278', 'article-title': 'Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis', 'volume': '50', 'author': 'Ellison', 'year': '1992', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis by Ellison (1992)
10.1159/000133633 / Cytogenet Cell Genet / Digitized and differentially shaded human chromosome ideograms for genomic applications by Francke (1994)
{'key': '10.1086/301932_bib6', 'first-page': '32', 'article-title': "Rett's syndrome: a progressive developmental disability in girls", 'volume': '6', 'author': 'Holm', 'year': '1985', 'journal-title': 'J Dev Behav Pediatr'} / J Dev Behav Pediatr / Rett's syndrome: a progressive developmental disability in girls by Holm (1985)
10.1101/gr.7.3.210 / Genome Res / X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content by Nagaraja (1997)
10.1086/515525 / Am J Hum Genet / A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map by Schanen (1997)
10.1177/088307389801300507 / J Child Neurol / Neonatal encephalopathy in two male children in families with recurrent Rett syndrome by Schanen (1998)

Dates

Type	When
Created	23 years, 1 month ago (July 26, 2002, 10:47 a.m.)
Deposited	6 years, 4 months ago (April 11, 2019, 9:27 a.m.)
Indexed	11 months, 3 weeks ago (Sept. 15, 2024, 12:35 p.m.)
Issued	27 years, 2 months ago (July 1, 1998)
Published	27 years, 2 months ago (July 1, 1998)
Published Print	27 years, 2 months ago (July 1, 1998)

Funders 0

None

BibTeX

@article{Schanen_1998, title={A Severely Affected Male Born into a Rett Syndrome Kindred Supports X-Linked Inheritance and Allows Extension of the Exclusion Map}, volume={63}, ISSN={0002-9297}, url={http://dx.doi.org/10.1086/301932}, DOI={10.1086/301932}, number={1}, journal={The American Journal of Human Genetics}, publisher={Elsevier BV}, author={Schanen, Carolyn and Francke, Uta}, year={1998}, month=jul, pages={267–269} }

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