Search research articles
Contact Us
Filters
Showing results (51-60 of 114) with videos related to
Page
of 12
Sort By:
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
August 1, 1986
[Ultrasound findings as a sign of fetal triploidy]
W Holzgreve, P Miny, A Holzgreve, et al.
Prenatal Diagnosis
|
September 1, 1989
Chromosome mosaicism of the placenta--a cause of developmental failure of the fetus?
E Schwinger, E Seidl, F Klink, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
October 1, 1981
[Prenatal differential diagnosis in elevated alpha-fetoprotein concentration in the amniotic fluid (author's transl)]
M Cremer, W Schmidt, T Voigtländer, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
February 26, 1998
Cystic hygroma as an early first-trimester ultrasound marker for recurrent Fryns' syndrome
I M Hösli, S Tercanli, H Rehder, et al.
Clinical Genetics
|
December 1, 1984
Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology
U Froster-Iskenius, W Coerdt, H Rehder, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
A new autosomal recessive skeletal dysplasia syndrome--prenatal diagnosis and histopathology
W Fuhrmann, A Fuhrmann-Rieger, V Jovanović, et al.
American Journal of Medical Genetics
|
October 1, 1993
Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings
U G Froster, H Rehder, W Höhn, et al.
European Journal of Pediatrics
|
December 1, 1984
Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformations
W Grote, H Rehder, D Weisner, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie
|
September 1, 1996
[Possibilities for false-negative findings in trisomy 21 screening with FISH]
B Fritz, B Van Oorschot, E Latta, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1982
[Holoprosencephaly-arhinencephaly complex in chromosome abnormalities compared to other causes]
F Gullotta, H Rehder, A Gropp, et al.
Page
of 12
Search research articles
Search
Showing results (51-60 of 114) with videos related to
Sort By:
Page
of 12
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
August 1, 1986
[Ultrasound findings as a sign of fetal triploidy]
W Holzgreve, P Miny, A Holzgreve, et al.
Prenatal Diagnosis
|
September 1, 1989
Chromosome mosaicism of the placenta--a cause of developmental failure of the fetus?
E Schwinger, E Seidl, F Klink, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
October 1, 1981
[Prenatal differential diagnosis in elevated alpha-fetoprotein concentration in the amniotic fluid (author's transl)]
M Cremer, W Schmidt, T Voigtländer, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
February 26, 1998
Cystic hygroma as an early first-trimester ultrasound marker for recurrent Fryns' syndrome
I M Hösli, S Tercanli, H Rehder, et al.
Clinical Genetics
|
December 1, 1984
Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology
U Froster-Iskenius, W Coerdt, H Rehder, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
A new autosomal recessive skeletal dysplasia syndrome--prenatal diagnosis and histopathology
W Fuhrmann, A Fuhrmann-Rieger, V Jovanović, et al.
American Journal of Medical Genetics
|
October 1, 1993
Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings
U G Froster, H Rehder, W Höhn, et al.
European Journal of Pediatrics
|
December 1, 1984
Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformations
W Grote, H Rehder, D Weisner, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie
|
September 1, 1996
[Possibilities for false-negative findings in trisomy 21 screening with FISH]
B Fritz, B Van Oorschot, E Latta, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie
|
January 1, 1982
[Holoprosencephaly-arhinencephaly complex in chromosome abnormalities compared to other causes]
F Gullotta, H Rehder, A Gropp, et al.
Page
of 12