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1.
Risk of pre-eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case-control study.
BJOG
; 128(1): 55-65, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32741103
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IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.
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Bilateral distal fibula fractures in a woman on long-term bisphosphonate therapy.
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Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.
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10.
Integrated human genome-wide maps constructed using the CEPH reference panel.
Nat Genet
; 6(4): 391-3, 1994 Apr.
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A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD.
Nat Genet
; 19(2): 167-70, 1998 Jun.
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Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.
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; 14(4): 392-9, 1996 Dec.
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Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
Nat Genet
; 2(1): 46-9, 1992 Sep.
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Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.
Nat Genet
; 26(1): 19-20, 2000 Sep.
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DNA methylation differences in monozygotic twins with Van der Woude syndrome.
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Clinical findings in patients with GLI2 mutations--phenotypic variability.
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Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus.
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Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.
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Global oral health inequalities: challenges in the prevention and management of orofacial clefts and potential solutions.
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Folic acid and orofacial clefts: a review of the evidence.
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