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Klinische Padiatrie
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July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]
G Schmid, F Haverkamp, J Rechmann, et al.
Annales De Genetique
|
June 9, 2004
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions
K Bosse, T Eggermann, K Van der Ven, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
December 1, 1988
Prenatal diagnosis and management in fetuses with cystic hygromata colli
U Gembruch, M Hansmann, R Bald, et al.
Klinische Padiatrie
|
November 1, 1972
[E 18 ring chromosome--case report and review]
K P Grosse, G Schwanitz, H D Rott, et al.
Zeitschrift Fur Kardiologie
|
February 1, 1990
[Fetal echocardiography and clinical genetics--a close correlation]
K Zerres, U Gembruch, G Schwanitz, et al.
Journal De Genetique Humaine
|
October 1, 1979
[Recessive microencephaly linked to the X chromosome]
Y Deshaies, H D Rott, H F Wissmuller, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1977
Duplication deficiency of an X-chromosome with and without 45,X mosaicism in three girls. Cytogenetic, clinical, and hormonal findings
G Schwanitz, H U Tietze, R A Pfeiffer, et al.
Klinische Padiatrie
|
January 1, 1999
[Undescended testis and hypospadia in sex chromosomal aberrations]
R Raff, R Schubert, G Schwanitz, et al.
Human Genetics
|
February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction
T Eggermann, M M Nöthen, B Eiben, et al.
Human Genetics
|
October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)
M M Nöthen, T Eggermann, J Erdmann, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 123) with videos related to
Sort By:
Page
of 13
Klinische Padiatrie
|
July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]
G Schmid, F Haverkamp, J Rechmann, et al.
Annales De Genetique
|
June 9, 2004
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions
K Bosse, T Eggermann, K Van der Ven, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
December 1, 1988
Prenatal diagnosis and management in fetuses with cystic hygromata colli
U Gembruch, M Hansmann, R Bald, et al.
Klinische Padiatrie
|
November 1, 1972
[E 18 ring chromosome--case report and review]
K P Grosse, G Schwanitz, H D Rott, et al.
Zeitschrift Fur Kardiologie
|
February 1, 1990
[Fetal echocardiography and clinical genetics--a close correlation]
K Zerres, U Gembruch, G Schwanitz, et al.
Journal De Genetique Humaine
|
October 1, 1979
[Recessive microencephaly linked to the X chromosome]
Y Deshaies, H D Rott, H F Wissmuller, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1977
Duplication deficiency of an X-chromosome with and without 45,X mosaicism in three girls. Cytogenetic, clinical, and hormonal findings
G Schwanitz, H U Tietze, R A Pfeiffer, et al.
Klinische Padiatrie
|
January 1, 1999
[Undescended testis and hypospadia in sex chromosomal aberrations]
R Raff, R Schubert, G Schwanitz, et al.
Human Genetics
|
February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction
T Eggermann, M M Nöthen, B Eiben, et al.
Human Genetics
|
October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)
M M Nöthen, T Eggermann, J Erdmann, et al.
Page
of 13