Sigrun Fuchs: search on Z-Library

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1

Spectrum of the acrocallosal syndrome

Rainer Koenig, Alexia Bach, Ulrike Woelki, Karl-Heinz Grzeschik, Sigrun Fuchs

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 308 KB

english, 2002

2

Simpson-Golabi-Behmel syndrome with severe cardiac arrhythmias

Dr. Rainer König, Sigrun Fuchs, Christoph Kern, Ulrich Langenbeck

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 771 KB

english, 1991

3

Quinacrine mustard fluorescence of a second Y chromosome in a Y-autosomal translocation

Sabine Fründ, Thea Koske-Westphal, Sigrun Fuchs-Mecke, Eberhard Passarge

Journal:

Year:

1972

Language:

english

File:

PDF, 473 KB

english, 1972

4

SHORT syndrome

Koenig, Rainer, Brendel, Leticia, Fuchs, Sigrun

Journal:

Clinical Dysmorphology

Year:

2003

Language:

english

File:

PDF, 209 KB

english, 2003

5

Quality Improvement Initiative for Severe Sepsis and Septic Shock Reduces 90-Day Mortality

Scheer, Christian S., Fuchs, Christian, Kuhn, Sven-Olaf, Vollmer, Marcus, Rehberg, Sebastian, Friesecke, Sigrun, Abel, Peter, Balau, Veronika, Bandt, Christoph, Meissner, Konrad, Hahnenkamp, Klaus, Gr

Journal:

Critical Care Medicine

Year:

2017

Language:

english

File:

PDF, 544 KB

english, 2017

6

SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders

Jürgen Kohlhase, David Chitayat, Dieter Kotzot, Serdar Ceylaner, Ursula G. Froster, Sigrun Fuchs, Tara Montgomery, Bernd Rösler

Journal:

Year:

2005

Language:

english

File:

PDF, 192 KB

english, 2005

7

OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs

Haug, Karsten, Khan, Saima, Fuchs, Sigrun, K�nig, Rainer

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 231 KB

english, 2000

8

A second case of Devriendt syndrome

Koenig, Rainer, Meinecke, Peter, Fuchs, Sigrun

Journal:

Clinical Dysmorphology

Year:

2005

Language:

english

File:

PDF, 194 KB

english, 2005

9

Bilateral congenital diaphragmatic hernia: Differentiation between Pallister-Killian and Fryns syndromes

Alex Veldman, Rolf Schlösser, Antje Allendorf, Doris Fischer, Klaus Heller, Beate Schaeff, Sigrun Fuchs

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 36 KB

english, 2002

10

Osteopathia striata with cranial sclerosis: Variable expressivity in a four generation pedigree

König, Rainer, Dukiet, Christof, Dörries, Andrea, Zabel, Bernhard, Fuchs, Sigrun

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 609 KB

1996

11

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

Türkmen, Seval, Gillessen-Kaesbach, Gabriele, Meinecke, Peter, Albrecht, Beate, Neumann, Luitgard M, Hesse, Volker, Palanduz, Sükrü, Balg, Stefanie, Majewski, Frank, Fuchs, Sigrun

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 166 KB

english, 2003

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