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Journal Abstract Search

75 related items for PubMed ID: 8923945

  • 1. Pattern of malformations in the axial skeleton in human trisomy 18 fetuses.
    Kjaer I, Keeling JW, Hansen BF.
    Am J Med Genet; 1996 Nov 11; 65(4):332-6. PubMed ID: 8923945
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  • 2. Pattern of malformations in the axial skeleton in human trisomy 13 fetuses.
    Kjaer I, Keeling JW, Fischer Hansen B.
    Am J Med Genet; 1997 Jun 27; 70(4):421-6. PubMed ID: 9182786
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  • 3. Pattern of malformations in the axial skeleton in human trisomy 21 fetuses.
    Keeling JW, Hansen BF, Kjaer I.
    Am J Med Genet; 1997 Feb 11; 68(4):466-71. PubMed ID: 9021023
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  • 4. Pattern of malformations in the axial skeleton in human triploid fetuses.
    Kjaer I, Keeling JW, Smith NM, Hansen BF.
    Am J Med Genet; 1997 Oct 17; 72(2):216-21. PubMed ID: 9382146
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  • 7. Skeletal abnormalities in fetuses with Down's syndrome: a radiographic post-mortem study.
    Stempfle N, Huten Y, Fredouille C, Brisse H, Nessmann C.
    Pediatr Radiol; 1999 Sep 17; 29(9):682-8. PubMed ID: 10460330
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  • 8. A histological and radiological investigation of the nasal bone in fetuses with Down syndrome.
    Tuxen A, Keeling JW, Reintoft I, Fischer Hansen B, Nolting D, Kjaer I.
    Ultrasound Obstet Gynecol; 2003 Jul 17; 22(1):22-6. PubMed ID: 12858297
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  • 9. Axial skeleton and pituitary gland in human fetuses with spina bifida and cranial encephalocele.
    Kjaer I, Hansen BF, Keeling JW.
    Pediatr Pathol Lab Med; 1996 Jul 17; 16(6):909-26. PubMed ID: 9025889
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  • 10. Prenatal development of the normal human vertebral corpora in different segments of the spine.
    Nolting D, Hansen BF, Keeling J, Kjaer I.
    Spine (Phila Pa 1976); 1998 Nov 01; 23(21):2265-71. PubMed ID: 9820904
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  • 11. Segmentation defects of the human axial skeleton without dysostoses or skeletal dysplasias.
    Bates AW, Nale K.
    Fetal Pediatr Pathol; 2005 Nov 01; 24(2):121-7. PubMed ID: 16243756
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  • 12. Pituitary gland and sella turcica in human trisomy 18 fetuses.
    Kjaer I, Keeling JW, Reintoft I, Hjalgrim H, Nolting D, Fischer Hansen B.
    Am J Med Genet; 1998 Feb 26; 76(1):87-92. PubMed ID: 9508072
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  • 13. Nasal bone length in trisomy 18, triploidy and Turner syndrome analyzed on postmortem radiographs.
    Mentz RG, Engel U, Kjaer I.
    Ultrasound Obstet Gynecol; 2009 Nov 26; 34(5):607-8. PubMed ID: 19852045
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  • 14. Skeletal malformations in fetuses with Meckel syndrome.
    Kjaer KW, Fischer Hansen B, Keeling JW, Kjaer I.
    Am J Med Genet; 1999 Jun 11; 84(5):469-75. PubMed ID: 10360401
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  • 17. Significance of cardiovascular malformations in cystic hygroma: a new interpretation of the pathogenesis.
    Miyabara S, Sugihara H, Maehara N, Shouno H, Tasaki H, Yoshida K, Saito N, Kayama F, Ibara S, Suzumori K.
    Am J Med Genet; 1989 Dec 11; 34(4):489-501. PubMed ID: 2533851
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  • 18. Cervical vertebrae, cranial base, and mandibular retrognathia in human triploid fetuses.
    Sonnesen L, Nolting D, Engel U, Kjaer I.
    Am J Med Genet A; 2009 Feb 11; 149A(2):177-87. PubMed ID: 19161148
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  • 20. Genetically induced abnormal cranial development in human trisomy 18 with holoprosencephaly: comparisons with the normal tempo of osteogenic-neural development.
    Reid SN, Ziermann JM, Gondré-Lewis MC.
    J Anat; 2015 Jul 11; 227(1):21-33. PubMed ID: 26018729
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