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Year | Number of Results |
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1964 | 1 |
1998 | 2 |
2024 | 0 |
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The type XI collagenopathies.
Pediatr Radiol. 1998 Oct;28(10):745-50. doi: 10.1007/s002470050459.
Pediatr Radiol. 1998.
PMID: 9799295
Review.
[SIMULTANEOUS OCCURRANCE OF THE PIERRE ROBIN SYNDROME AND FETAL CHONDRODYSPLASIA].
WEISSENBACHER G, ZWEYMUELLER E.
WEISSENBACHER G, et al.
Monatsschr Kinderheilkd (1902). 1964 Jun;112:315-7.
Monatsschr Kinderheilkd (1902). 1964.
PMID: 14234962
German.
No abstract available.
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Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome).
Pihlajamaa T, Prockop DJ, Faber J, Winterpacht A, Zabel B, Giedion A, Wiesbauer P, Spranger J, Ala-Kokko L.
Pihlajamaa T, et al.
Am J Med Genet. 1998 Nov 2;80(2):115-20. doi: 10.1002/(sici)1096-8628(19981102)80:2<115::aid-ajmg5>3.0.co;2-o.
Am J Med Genet. 1998.
PMID: 9805126
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