Sabine Stengel-Rutkowski: search on Z-Library

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1

A familial deletion in the Prader-Willi syndrome region including the imprinting control region

Simone Schuffenhauer, Tina Buchholz, Sabine Stengel-Rutkowski, Karin Buiting, Heinrich Schmidt, Thomas Meitinger

Journal:

Year:

1996

Language:

english

File:

PDF, 500 KB

english, 1996

2

Congenital diaphragmatic hernia in the Brachmann-de Lange syndrome

Christopher Cunniff, Cynthia J. R. Curry, John C. Carey, John M. Graham Jr., Charles A. Williams, Sabine Stengel-Rutkowski, Sabine Lüttgen, Peter Meinecke

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 407 KB

english, 1993

3

Further delineation of the branchio-oculo-facial syndrome

Angela E. Lin, Robert J. Gorlin, Iosif W. Lurie, Han G. Brunner, Ineke van der Burgt, Irena V. Naumchik, Natalja V. Rumyantseva, Sabine Stengel-Rutkowski, Kenneth Rosenbaum, Peter Meinecke, Dietmar Mu

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 1.73 MB

english, 1995

4

Gonadendysgenesie mit ungewöhnlicher Strukturanomalie eines X-Chromosoms (45,X/46,XXq+)

A. Dollmann, W. Nocke, Sabine Stengel-Rutkowski

Journal:

Year:

1972

File:

PDF, 892 KB

1972

5

A reanalysis of the New York State prenatal diagnosis data on Down's syndrome and paternal age effects

Eeva Stene, Jon Stene, Sabine Stengel-Rutkowski

Journal:

Year:

1987

Language:

english

File:

PDF, 430 KB

english, 1987

6

On methodological issues regarding 47,+21 paternal age data

Eeva Stene, Jon Stene, Sabine Stengel-Rutkowski

Journal:

Year:

1987

Language:

english

File:

PDF, 119 KB

english, 1987

7

10.1038/2484

Brown, Stephen A., Warburton, Dorothy, Brown, Lucia Y., Yu, Chih-yu, Roeder, Elizabeth R., Stengel-Rutkowski, Sabine, Hennekam, Raoul C.M., Muenke, Maximilian

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 195 KB

english, 1998

8

Experiences with risk estimates for carriers of chromosomal reciprocal translocations

Alina T. Midro, Sabine Stengel-Rutkowski, Jon Stene

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 874 KB

english, 1992

9

3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndrome

Konrad Oexle, Maja Hempel, Anna Jauch, Thomas Meitinger, Núria Rivera-Brugués, Sabine Stengel-Rutkowski, Tim Strom

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 501 KB

english, 2011

10

KLINEFELTER'S SYNDROME IN A FETUS

Murken, Jan-Diether, Stengel-Rutkowski, Sabine, Walther, Joachim-Ulrich, Westenfelder, SilviaR., Remberger, K.H., Zimmer, Fritz

Journal:

Year:

1974

Language:

english

File:

PDF, 170 KB

english, 1974