scholarly article | Q13442814 |
P2093 | author name string | Imaizumi K | |
Stephens RS | |||
Matsuno M | |||
Davies AF | |||
Kuroki Y | |||
Ragoussis J | |||
Mirza G | |||
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Eleven new cases of del(9p) and features from 80 cases | Q33682033 | ||
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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;9q22.3 | Q57813505 | ||
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6 | Q69906191 | ||
Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region | Q72144569 | ||
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 gene | Q74237599 | ||
Whom would you trust with your genetic information? | Q74766743 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 857-861 | |
P577 | publication date | 1998-10-01 | |
P1433 | published in | Journal of Medical Genetics | Q14640281 |
P1476 | title | Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting | |
P478 | volume | 35 |
Q35866596 | Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1 |
Q34657339 | Gene/environment causes of cleft lip and/or palate |
Q39023014 | Genetic Advances in the Understanding of Microtia |
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