E-LIB Suche - Ergebnisse für: Zirn, Birgit

1

Pränataldiagnostik zur Detektion chromosomaler Aberratione..:

Bach, Veronika Franziska , 2022

2

Epidemiology of inherited epidermolysis bullosa in Germany:

Has, Cristina ; Hess, Moritz ; Anemüller, Waltraud...
Journal of the European Academy of Dermatology and Venereology. 37 (2022) 2 - p. 402-410 , 2022

Link: https://doi.org/10.1111/..

3

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/..

4

CADA: phenotype-driven gene prioritization based on a case-..:

Peng, Chengyao ; Dieck, Simon ; Schmid, Alexander...
NAR Genomics and Bioinformatics. 3 (2021) 3 - p. , 2021

Link: https://doi.org/10.1093/..

5

A Basic principles:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 1-15 , 2019

Link: https://doi.org/10.1007/..

6

D Inheritance patterns:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 81-91 , 2019

Link: https://doi.org/10.1007/..

7

B Cytogenetics:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 17-63 , 2019

Link: https://doi.org/10.1007/..

8

F Cancer:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 107-127 , 2019

Link: https://doi.org/10.1007/..

9

Clinical report of 8 patients with 49,XXXXY syndrome: Delin..:

Burgemeister, Anna L. ; Daumiller, Eva ; du Bois, Gabriele...
European Journal of Medical Genetics. 62 (2019) 3 - p. 210-216 , 2019

Link: https://doi.org/10.1016/..

10

Guide for Genetic Consultation:

Zirn, Birgit ; Mehnert, Karl - 1st ed. 2019 . , 2019

Link: https://doi.org/10.1007/..

11

G Common disorders:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 129-187 , 2019

Link: https://doi.org/10.1007/..

12

E Reproduction:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 93-105 , 2019

Link: https://doi.org/10.1007/..

13

Clinical long-time course, novel mutations and genotype-phe..:

Geis, Tobias ; Rödl, Tanja ; Topaloğlu, Haluk...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

14

C Prenatal diagnostics:

, In: Guide for Genetic Consultation,

Zirn, Birgit ; Mehnert, Karl - p. 65-79 , 2019

Link: https://doi.org/10.1007/..

15

Continuing role for classical cytogenetics: Case report of ..:

Burgemeister, Anna Lena ; Daumiller, Eva ; Dietze‐Armana, Ilona...
American Journal of Medical Genetics Part A. 173 (2017) 3 - p. 727-732 , 2017

Link: https://doi.org/10.1002/..