Yunis-Varon syndrome: the first case of German origin (English)
- New search for: Rabe, H.
- New search for: Brune, T.
- New search for: Rossi, R.
- New search for: Steinhorst, V.
- New search for: Jorch, G.
- New search for: Horst, J.
- New search for: Wittwer, B.
- New search for: Rabe, H.
- New search for: Brune, T.
- New search for: Rossi, R.
- New search for: Steinhorst, V.
- New search for: Jorch, G.
- New search for: Horst, J.
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In:
CLINICAL DYSMORPHOLOGY
;
5
, 3
;
217-222
;
1996
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ISSN:
- Article (Journal) / Print
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Title:Yunis-Varon syndrome: the first case of German origin
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Contributors:Rabe, H. ( author ) / Brune, T. ( author ) / Rossi, R. ( author ) / Steinhorst, V. ( author ) / Jorch, G. ( author ) / Horst, J. ( author ) / Wittwer, B. ( author )
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Published in:CLINICAL DYSMORPHOLOGY ; 5, 3 ; 217-222
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Publisher:
- New search for: CHAPMAN & HALL
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Publication date:1996-01-01
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Size:6 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 616
- Further information on Dewey Decimal Classification
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Classification:
DDC: 616 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 5, Issue 3
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 187
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Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanismVan Meter, T. D. / Weaver, D. D. et al. | 1996
- 197
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Spondylo-meta-epiphyseal dysplasia, short limb, abnormal calcification typeAl-Gazali, L. I. / Bakalinova, D. / Sztriha, L. et al. | 1996
- 207
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Nance-Sweeney chondrodysplasia - a further case?Rosser, E. M. / Hall, C. M. / Harper, J. / Lacour, M. / Baraitser, M. et al. | 1996
- 213
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A new lethal chondrodysplasia with platyspondyly, long bone angulation and mixed bone densitySeller, M. J. / Berry, A. C. / Maxwell, D. / McLennan, A. / Hall, C. M. et al. | 1996
- 217
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Yunis-Varon syndrome: the first case of German originRabe, H. / Brune, T. / Rossi, R. / Steinhorst, V. / Jorch, G. / Horst, J. / Wittwer, B. et al. | 1996
- 223
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Hypertrichosis, coarse face, brachydactyly, obesity and mental retardationPavone, L. / Rizzo, R. / Ruggieri, M. / Sorge, G. et al. | 1996
- 231
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New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasiaTemtamy, S. A. / Salam, M. A. / Aboul-Ezz, E. H. A. / Hussein, H. A. / Helmy, S. A. H. / Shalash, B. A. et al. | 1996
- 241
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Three infants of diabetic mothers with malformations of left-right asymmetry - further evidence for the aetiological role of diabetes in this malformation spectrumSlavotinek, A. / Hellen, E. / Gould, S. / Coghill, S. B. / Huson, S. M. / Hurst, J. A. et al. | 1996
- 249
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Setleis syndrome: autosomal recessive or autosomal dominant inheritance?Al-Gazali, L. I. / Al-Talabani, J. et al. | 1996
- 255
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Isolated macrodactyly and Proteus syndromeLacombe, D. / Battin, J. et al. | 1996
- 259
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Blepharophimosis syndrome (BPES) and additional abnormalities in a female with a balanced X:3 translocationKarimi-Nejada, A. / Karimi-Nejad, R. / Najafi, H. / Karimi-Nejad, M. H. et al. | 1996
- 263
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Craniosynostosis with Marfan syndrome, hand and foot anomaliesShah, A. M. / Chattopadhyay, A. / Kher, A. / Bharucha, B. A. / Karapurkar, A. P. et al. | 1996
- 267
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Colonic and pyloric atresia coexisting with isolated segmental dilatation of the ileum: an exceedingly rare triple anomalySenocak, M. E. / Arda, I. S. / Bueyuekpamukcu, N. et al. | 1996
- 271
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Bardet-Biedl Syndrome: delayed diagnosis in a child with Hirschsprung diseaseIslek, I. / Kuecuekoduek, S. / Erkan, D. / Bernay, F. / Kalayci, A. G. / Goerk, S. / Kandemir, B. / Guerses, N. et al. | 1996
- 275
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Pili bifurcati: occurring in association with the mosaic trisomy 8 syndromeBreslau-Siderius, L. J. / Beemer, F. A. / Boom, B. W. et al. | 1996