Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: An oral clefting model supporting the Pierre-Robin sequence

Teratology

Volumn 65, Issue 3, 2002, Pages 116-120

  Ricks, James E ^a   Ryder, Victoria M ^a   Bridgewater, Laura C ^a   Schaalje, Bruce ^a   Seegmiller, Robert E ^a  

^a BRIGHAM YOUNG UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CLEFT PALATE; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; EMBRYO; GENE MUTATION; GENOTYPE; GROWTH RETARDATION; HOMOZYGOSITY; MACROGLOSSIA; MICROGNATHIA; MICROMELIA; MOUSE; NONHUMAN; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL;

ANIMALS; CLEFT PALATE; COLLAGEN TYPE II; HOMOZYGOTE; MANDIBLE; MICE; MICE, INBRED C3H; MICROGNATHISM; PALATE; PIERRE ROBIN SYNDROME; SEQUENCE DELETION;

EID: 0036183541     PISSN: 00403709     EISSN: None     Source Type: Journal    
DOI: 10.1002/tera.10022     Document Type: Article

References (29)

1. PCR assay confirms diagnosis in syndrome with variably expressed phenotype: Mutation detection in Stickler syndrome
2. Linkage study in a large pedigree with Stickler syndrome: Exclusion of COL2A1 as the mutant gene
3. Disproportionate micromelia (Dmm): An incomplete dominant mouse dwarfism with abnormal cartilage matrix
4. Chondrodystrophic mice with coincidental agnathia: Evidence for the tongue obstruction hypothesis in cleft palate
5. The Robin anomolad: Its non-specificity and associated syndromes
6. Correlation between alterations in Meckel's cartilage and induction of cleft palate with beta-aminoproprionitrile in the rat
7. Craniofacial growth during human secondary palate formation and potential relevance of experimental cleft palate observations
8. Abnormal head posture associated with induction of cleft palate by methylmercury in C57BL/6J mice
9. Selective inhibition of mandibular growth and induction of cleft palate by diazo-oxo-norleucine (DON) in the rat
10. Prevalence of selected pediatric conditions in children with Pierre-Robin sequence
11. The Stickler syndrome: Evidence for close linkage to the structural gene for type II collagen
12. Incidence of cleft lip and palate and risks of additional malformations
13. Morphology of isolated cleft palate in children, including Robin sequence, treated with one or two-stage operations
14. Treatment of cleft palate associated with Robin sequence: Appraisal of risk factors
15. The mechanism of palatal clefting in the Col11al mutant mouse
16. Etiopathogenesis of isolated Robin sequence
17. Coenzyme competition and precursor specificity during teratogenesis induced by 6-aminonicotinamide
18. Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1
19. Beyond Pierre-Robin sequence
20. Robin sequence: Changes in thinking leading to changes in patient care
21. Histological and fine structural changes during chondrogenesis in micromelia induced by 6-aminonicotinamide
22. Histochemical, immunofluorescence and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice
23. Mandibular growth retardation as a cause of cleft palate in mice homozygous for the chondrodysplasia gene
24. Clinical and molecular genetics of Stickler syndrome
25. Classification and birth prevalence of orofacial clefts
26. Strain differences in susceptibility to teratogenesis. Survey of spontaneously occurring malformations in mice
27. Pierre-Robin sequence and severe mental retardation with chaotic behavior associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)
28. Ultrasonic diagnosis of amniotic band syndrome in pregnancy