About: Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991

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About: Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991 Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	наукова стаття, опублікована в 1991 (uk) im Jahr 1991 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q93508047-31718F22-E5F5-4543-B796-F58B89B8CCF2
publication date	1991-01-01 00:00:00Z (xsd:dateTime)
rdfs:label	Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991 (en)
skos:prefLabel	Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991 (en)
name	Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991 (en)
title	wds:Q93508047-984C7248-4349-4E38-9597-A4FB1EF3D988
title	Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991 (en)
page(s)	wds:Q93508047-0E65DD25-E6D6-471F-8E30-427A1BA5B1C1
page(s)	986-2156
instance of	wds:Q93508047-66AFD339-2AAC-4E98-A3B2-7A4E5CC00BF6
instance of	scholarly article
PubMed ID	wds:Q93508047-BB3A46C4-0F90-4CCF-AAEB-00D8BF72DEB8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1685704
PubMed ID	1685704
published in	wds:Q93508047-C91AA66F-B624-42FC-8EBC-D4D46DBD7035
published in	Cytogenetics and Cell Genetics
issue	wds:Q93508047-93989A6E-1664-4941-81ED-29C9704D5BA3
volume	wds:Q93508047-D8A78933-39FB-4606-968A-8656BDC905AB
issue	3-4
volume	58
DOI	wds:Q93508047-089971D0-EC17-471D-AD24-87B7F4939A17
DOI	http://dx.doi.org/10.1159/000133716
DOI	10.1159/000133716
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q93508047
is cites work of	Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Physical mapping of the holoprosencephaly critical region in 18p11.3 Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Assignment of the genes encoding human interleukin-8 receptor types 1 and 2 and an interleukin-8 receptor pseudogene to chromosome 2q35 Multilocus polycystic disease Holoprosencephaly: a paradigm for the complex genetics of brain development. Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12 Functional analysis of mutations in TGIF associated with holoprosencephaly A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disorders Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1 Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. Molecular cloning of a cDNA encoding mouse A15, a member of the transmembrane 4 superfamily, and its preferential expression in brain neurons Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly First trimester diagnosis of holoprosencephaly and cyclopia with triploidy by transvaginal three-dimensional ultrasonography A somatic cell hybrid panel for regional mapping of human chromosome 18. Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly Localization of PMP-22 gene (candidate gene for the Charcot-Marie-Tooth disease 1a) to band 17p11.2 by direct r-banding fluoreschenceIn situ hybridization Kabuki make-up syndrome is not caused by microdeletion close to the van der Woude syndrome critical region at 1q32-q41 Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat Agnathia-holoprosencephaly-situs inversus Preaxial polydactyly in an infant with Down's syndrome
is cites work of	wds:Q24672141-F9FA8A12-8474-45D4-9AF5-CCD3D215EC69 wds:Q67479716-C5C0E4EE-F317-4195-A053-508BB60C231F wds:Q73953416-91F85D5B-5A94-491D-A67A-CE64E184AC74 wds:Q24681018-C12E550D-BEC7-4AE8-A691-356868C04A5F wds:Q33595214-07DB7EC1-08B5-4834-B218-05CDD1A1B2A0 wds:Q48058539-DD3C23D5-2F16-4FF5-BEB2-C25436C53951 wds:Q41567717-2C30400C-C8EA-4E1E-9D65-DC0FECFE12D4 wds:Q78247602-D32FE827-70EE-496D-873D-64C142F47383 wds:Q24514983-B204FF70-DA4F-4C6D-9285-9788E4680056 wds:Q24306411-CE8D20E2-F184-43C4-A597-9B92A78149DC wds:Q44412153-23EC9D26-529F-4128-B6FC-06CC11A33E65 wds:Q73290757-D4DCCD8D-24FF-4566-945C-7C0B90C60183 wds:Q28261277-238BB543-9ACE-4EC2-AACA-EA0C00C8316A wds:Q33679460-3304ECD2-F0FD-4CB3-8100-CE11B2919C28 wds:Q33679707-F6BE5C3E-1127-4215-9932-85296BFFD069 wds:Q35889456-C118A195-B737-4CA4-8B7F-0CF0B29F7C38 wds:Q33885240-83173A56-B51C-4B96-B33A-F75EC1D8D693 wds:Q28201871-A30004AA-48FC-4CB5-9DB2-38E3F3877912 wds:Q24671971-1EF9EEDA-B8E9-42DE-8FB7-265F8A916D16 wds:Q73651896-AD0E9856-96AF-4108-BB60-78632C351EF3 wds:Q93921147-7627576A-E7A4-4EA3-BEEE-D1039FA99691 wds:Q30495385-9047DBC5-2F3F-4AEE-BF7F-160BDFFA17EB wds:Q42805506-A08F4B1A-B4B9-49E5-9005-59F4D1269D88 wds:Q48400659-043D7931-9031-46D4-9F78-75C9EBF95F6F

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