Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting

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Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/JMG.35.10.857
P932PMC publication ID1051465
P698PubMed publication ID9783713
P5875ResearchGate publication ID13502070

P2093author name stringImaizumi K
Stephens RS
Matsuno M
Davies AF
Kuroki Y
Ragoussis J
Mirza G
P2860cites workTranscription factor AP-2 essential for cranial closure and craniofacial developmentQ28513302
Eleven new cases of del(9p) and features from 80 casesQ33682033
An integrated map of human chromosome 6p23.Q36812627
Partial deletion of chromosome 6p: delineation of the syndromeQ37773731
Associated malformations in infants with cleft lip and palate: a prospective, population-based study.Q51999824
A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.Q52007413
Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3Q57813505
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6Q69906191
Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the regionQ72144569
Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this geneQ74237599
Whom would you trust with your genetic information?Q74766743
P433issue10
P407language of work or nameEnglishQ1860
P304page(s)857-861
P577publication date1998-10-01
P1433published inJournal of Medical GeneticsQ14640281
P1476titleFurther evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting
P478volume35

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cites work (P2860)
Q35866596Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1
Q34657339Gene/environment causes of cleft lip and/or palate
Q39023014Genetic Advances in the Understanding of Microtia
Q33830886Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2.
Q28592776Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme
Q52618600Microtia: epidemiology and genetics.
Q24655503Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6
Q31104515QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

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