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Unger, Sheila
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1

Nosology of genetic skeletal disorders: 2023 revision:

Unger, Sheila ; Ferreira, Carlos R. ; Mortier, Geert R....
American Journal of Medical Genetics Part A.  191 (2023)  5 - p. 1164-1209 , 2023
Link: https://doi.org/10.1002/..
 
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2

Clinical and Molecular Diagnosis of Osteocraniostenosis in ..:

Rosato, Simonetta ; Unger, Sheila ; Campos-Xavier, Belinda...
Genes.  13 (2022)  2 - p. 261 , 2022
Link: https://doi.org/10.3390/..
 
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3

Analysis of missense variants in the human genome reveals w..:

Quinodoz, Mathieu ; Peter, Virginie G. ; Cisarova, Katarina...
The American Journal of Human Genetics.  109 (2022)  3 - p. 457-470 , 2022
Link: https://doi.org/10.1016/..
 
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4

Genetische Beratung: Konzepte Missverstndnisse Perspektiven:

Filges, Isabel ; Cichon, Sven ; Nouspikel, Thierry...
Schweizerische Ärztezeitung.  , 2022
Link: https://doi.org/10.4414/..
 
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5

Chondrodysplasia and growth failure in children after early..:

Botto, Lorenzo D. ; Meeths, Marie ; Campos‐Xavier, Belinda...
American Journal of Medical Genetics Part A.  185 (2021)  2 - p. 517-527 , 2021
Link: https://doi.org/10.1002/..
 
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6

Update Swiss guideline for counselling and testing for pred..:

Stoll, Susanna ; Unger, Sheila ; Azzarello-Burri, Silvia...
Swiss Medical Weekly.  151 (2021)  3738 - p. w30038 , 2021
Link: https://doi.org/10.4414/..
 
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7

Immune deficiency, autoimmune disease and intellectual disa..:

Atallah, Isis ; Quinodoz, Mathieu ; Campos‐Xavier, Belinda...
Clinical Genetics.  99 (2021)  6 - p. 780-788 , 2021
Link: https://doi.org/10.1111/..
 
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8

Cancer surveillance in children with Ollier Disease and Maf..:

Diezi, Manuel ; Zambelli, Pierre‐Yves ; Superti‐Furga, Andrea..
American Journal of Medical Genetics Part A.  185 (2021)  4 - p. 1338-1340 , 2021
Link: https://doi.org/10.1002/..
 
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9

Non-coding deletions identify Maenli lncRNA as a limb-speci..:

Allou, Lila ; Balzano, Sara ; Magg, Andreas...
Nature.  , 2021
Link: https://doi.org/10.1038/..
 
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10

Is height important for quality of life in children with sk..:

Lorne, Hortense ; Newman, Christopher J. ; Unger, Sheila
European Journal of Medical Genetics.  63 (2020)  4 - p. 103816 , 2020
Link: https://doi.org/10.1016/..
 
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11

Physicians communicating with women at genetic risk of brea..:

Fadda, Marta ; Chappuis, Pierre O. ; Katapodi, Maria C....
PLOS ONE.  15 (2020)  10 - p. e0240054 , 2020
Link: https://doi.org/10.1371/..
 
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12

Non-invasive prenatal testing leading to a maternal diagnos..:

Kumps, Camille ; Niel Bütschi, Florence ; Rapin, Blandine...
Journal of Human Genetics.  65 (2020)  11 - p. 1035-1038 , 2020
Link: https://doi.org/10.1038/..
 
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13

The Connective Tissue Disorder Associated with Recessive Va..:

Kumps, Camille ; Campos-Xavier, Belinda ; Hilhorst-Hofstee, Yvonne...
Genes.  11 (2020)  4 - p. 420 , 2020
Link: https://doi.org/10.3390/..
 
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14

Osteogenesis imperfecta: towards an individualised interdis..:

Aubry-Rozier, Bérengère ; Richard, Céline ; Unger, Sheila...
Swiss Medical Weekly.  150 (2020)  2728 - p. w20285 , 2020
Link: https://doi.org/10.4414/..
 
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15

Combined Lung and Liver Transplantation for Short Telomere ..:

Moschouri, Eleni ; Vionnet, Julien ; Giostra, Emiliano...
Liver Transplantation.  26 (2020)  6 - p. 840-844 , 2020
Link: https://doi.org/10.1002/..
 
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