Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;

McCorquodale, M.; Erickson, Robert P.; Robinson, M.; Roszczipka, K.

Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;

dc.contributor.author	McCorquodale, M.	en_US
dc.contributor.author	Erickson, Robert P.	en_US
dc.contributor.author	Robinson, M.	en_US
dc.contributor.author	Roszczipka, K.	en_US
dc.date.accessioned	2010-04-01T14:46:00Z
dc.date.available	2010-04-01T14:46:00Z
dc.date.issued	1980-06	en_US
dc.identifier.citation	McCorquodale, M.; Erickson, R. P.; Robinson, M.; Roszczipka, K. (1980). "Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;." Clinical Genetics 17(6): 409-414. <http://hdl.handle.net/2027.42/65214>	en_US
dc.identifier.issn	0009-9163	en_US
dc.identifier.issn	1399-0004	en_US
dc.identifier.uri	https://hdl.handle.net/2027.42/65214
dc.identifier.uri	http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7398112&dopt=citation	en_US
dc.format.extent	409117 bytes
dc.format.extent	3110 bytes
dc.format.mimetype	application/pdf
dc.format.mimetype	text/plain
dc.publisher	Blackwell Publishing Ltd	en_US
dc.rights	1980 Blackwell Munksgaard	en_US
dc.subject.other	Q14)	en_US
dc.subject.other	Birth Defects	en_US
dc.subject.other	Chromosomal Anomaly	en_US
dc.subject.other	Chromosomes (Human)	en_US
dc.subject.other	Cytogenetics (Human)	en_US
dc.subject.other	Dolichocephalic Skull	en_US
dc.subject.other	Familial Translocation	en_US
dc.subject.other	KleeblattschÄDel Anomaly	en_US
dc.subject.other	Partial Trisomy 13	en_US
dc.subject.other	3/13 Translocation	en_US
dc.title	Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;	en_US
dc.type	Article	en_US
dc.rights.robots	IndexNoFollow	en_US
dc.subject.hlbsecondlevel	Genetics	en_US
dc.subject.hlbtoplevel	Health Sciences	en_US
dc.description.peerreviewed	Peer Reviewed	en_US
dc.contributor.affiliationum	Medical College of Ohio at Toledo and University Hospital, Ann Arbor, Michigan, USA.	en_US
dc.identifier.pmid	7398112	en_US
dc.description.bitstreamurl	http://deepblue.lib.umich.edu/bitstream/2027.42/65214/1/j.1399-0004.1980.tb00171.x.pdf
dc.identifier.doi	10.1111/j.1399-0004.1980.tb00171.x	en_US
dc.identifier.source	Clinical Genetics	en_US
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dc.identifier.citedreference	Hauschtek, E. G. MÜrset, A. Prader & E. BÜhler ( 1966 ). Siblings with different types of chromosomal aberrations due to D/E trans-location of the mother. Cytogenetics 5, 281 – 294.	en_US
dc.identifier.citedreference	Jacobsen, P. M. Mikkelsen, A. Froland & A. Dupont ( 1966 ). Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cyto-genetic, and autoradiographic studies. Ann. hum. Genet. 29, 391402.	en_US
dc.identifier.citedreference	Kajii, T. J. Meylan & K. Mkamo ( 1974 ). Chromosome anomalies in three successive abortuses due to paternal translocation, t(13q -18q +). Cytogenet. Cell Genet. 13, 426 – 436.	en_US
dc.identifier.citedreference	Kaye, C. I. C. W. Booth, D. Meeker & H. Nadler ( 1977 ). Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy. Cleft Palate J. 14, 244 – 248.	en_US
dc.identifier.citedreference	Lewandowski, R. C. & J. J. Yunis ( 1977 ). Phenotypic mapping in man. New Chromosomal Syndromes, ed. J. J. Yunis New York, Academic Press, pp. 369 – 394.	en_US
dc.identifier.citedreference	Loevy, H. T. B. N. Jayaram, I. M. Rosenthal & R. Pildes ( 1977 ). Partial trisomy 13 associated wth cleft lip and cleft palate. Cleft Palate J. 14, 239 – 243.	en_US
dc.identifier.citedreference	Macintyre, M. N. W. I. Staples & J. J. Lapolla ( 1964 ). Partial D 1 trisomy in a child whose mother and maternal grandmother demonstrate a D/F translocation. Paper presented to the American Society of Human Genetics, Boulder, Col. August 1964 (Abstracts, p. 21).	en_US
dc.identifier.citedreference	Noel, B. B. Quack & M. O. Rethore ( 1976 ). Partial deletions and trisomies of chromosome 13. Mapping of bands associated with particular malformations. Clin. Genet. 9, 593 – 602.	en_US
dc.identifier.citedreference	Opitz, J. M. ( 1969 ). Familial anomalies in the Pierre Robin syndrome. Birth Defects: Original Article Serzes Vol. V, No. 2, 119.	en_US
dc.identifier.citedreference	Opitz, J. M. T. France, J. Herrmann & J. Spranger ( 1972 ). The Strickler Syndrome. New Engl. J. Med. 286, 546 – 547.	en_US
dc.identifier.citedreference	Patau, K. D. W. Smith, E. Therman, S. L. In-horn & H. P. Wagner ( 1960 ). Multiple congenital anomaly caused by an extra auto-some. Lancet i, 790 – 793.	en_US
dc.identifier.citedreference	Pedersen, C. ( 1976 ). Partial trisomy 15 as a result of an unbalanced 12/15 translocation in a patient with a cloverleaf skull anomaly. Clin. Genet. 9, 378 – 380.	en_US
dc.identifier.citedreference	Schinzel, A. W. Schmid & G. Murset ( 1974 ). Different forms of incomplete trisomy for the proximal and distal long arm. Report of three cases. Hum. Genet. 22, 287 – 298.	en_US
dc.identifier.citedreference	Schwanitz, G. K. P. Grosse, U. Semmelmayer & H. Manzold ( 1974 ). Partielle freie trisomie 13 in einer Familie mit balancierter Trans-Iokation (13q–16q+). Mschr. Kinderheilk. 122, 337 – 342.	en_US
dc.identifier.citedreference	Wilroy, R. S. R. L. Summit & P. R. Martens ( 1975 ). Partial trisomy for different segments of chromoso'me 13 in several individuals of the same family. Birth Dejects: Original Article Series Vol. XI, No. 5, 217 – 222.	en_US
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dc.owningcollname	Interdisciplinary and Peer-Reviewed

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