Search Results - "GLINSKI, L. P"

Prospective assessment of risks for cervicomedullary-junction compression in infants with achondroplasia by PAULI, R. M, HORTON, V. K, GLINSKI, L. P, REISER, C. A

“…Achondroplasia, the most common heritable skeletal dysplasia, may result in abnormality at the craniocervical junction, which is a potentially lethal problem…”
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Prevention of Fixed, Angular Kyphosis in Achondroplasia by Pauli, Richard M, Breed, Alan, Horton, V Kim, Glinski, Lisa P, Reiser, Catherine A

“…Transient kyphotic deformity arises in most infants with achondroplasia. In a minority, a fixed and angular kyphosis develops, which can cause serious…”
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Biophysical bases for delayed and aberrant motor development in young children with achondroplasia by Fowler, E S, Glinski, L P, Reiser, C A, Horton, V K, Pauli, R M

“…Achondroplasia, the most common skeletal dysplasia, is characterized by delayed and aberrant motoric development in childhood. Delays and aberrancy are…”
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Linkage of an autosomal dominant clefting syndrome (Van der Woude) to Loci on chromosome Iq by MURRAY, J. C, NISHIMURA, D. Y, GLINSKI, L. P, PAULI, R. M, NAKAMURA, Y, GREEN, P. P, SCHINZEL, A, BUETOW, K. H, ARDINGER, H. H, SPENCE, M. A, SPARKES, R. S, FALK, R. E, FALK, P. M, GARDNER, R. J. M, HARKNESS, E. M

“…Van der Woude syndrome (VWS) is an autosomal dominant disorder in which affected individuals have one or more of the following manifestations: cleft lip, cleft…”
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Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accident by Robertson, W L, Glinski, L P, Kirkpatrick, S J, Pauli, R M

“…A 7 1/2-year-old girl with arthrogryposis multiplex congenita of the amyoplasia type in association with intestinal atresias, gastroschisis, Möbius anomaly,…”
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