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Clinical Genetics
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February 1, 1993
A case of full triploidy (69,XXX) of paternal origin with unusually long survival time
S C Niemann-Seyde, H Rehder, B Zoll
Prenatal Diagnosis
|
May 1, 1990
Prenatal diagnosis and postnatal follow-up of a child with two de novo unrelated balanced reciprocal translocations
M Pruggmayer, B Zoll, M Leipoldt, et al.
Blut
|
January 1, 1990
Diagnosis of haemophilia B using the polymerase chain reaction
J Reiss, U Neufeldt, K Wieland, et al.
Journal of Neurology
|
July 1, 1991
Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissue
U Diedrich, S Soja, J Behnke, et al.
The British Journal of Dermatology
|
June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?
S Schauder, F Hanefeld, U M Noske, et al.
Clinical Genetics
|
October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generations
S C Niemann-Seyde, S W Eber, B Zoll
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Fetal alcohol syndrome in association with Rett syndrome
B Zoll, P Huppke, A Wessel, et al.
Der Nervenarzt
|
October 1, 1991
[Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers]
U Thies, K Schröder, B Bockel, et al.
Human Genetics
|
June 1, 1994
Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families
C Meyer-Kleine, M Otto, B Zoll, et al.
American Journal of Medical Genetics
|
December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus sampling
I Bartels, I Hansmann, U Holland, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
Clinical Genetics
|
February 1, 1993
A case of full triploidy (69,XXX) of paternal origin with unusually long survival time
S C Niemann-Seyde, H Rehder, B Zoll
Prenatal Diagnosis
|
May 1, 1990
Prenatal diagnosis and postnatal follow-up of a child with two de novo unrelated balanced reciprocal translocations
M Pruggmayer, B Zoll, M Leipoldt, et al.
Blut
|
January 1, 1990
Diagnosis of haemophilia B using the polymerase chain reaction
J Reiss, U Neufeldt, K Wieland, et al.
Journal of Neurology
|
July 1, 1991
Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissue
U Diedrich, S Soja, J Behnke, et al.
The British Journal of Dermatology
|
June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?
S Schauder, F Hanefeld, U M Noske, et al.
Clinical Genetics
|
October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generations
S C Niemann-Seyde, S W Eber, B Zoll
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Fetal alcohol syndrome in association with Rett syndrome
B Zoll, P Huppke, A Wessel, et al.
Der Nervenarzt
|
October 1, 1991
[Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers]
U Thies, K Schröder, B Bockel, et al.
Human Genetics
|
June 1, 1994
Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families
C Meyer-Kleine, M Otto, B Zoll, et al.
American Journal of Medical Genetics
|
December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus sampling
I Bartels, I Hansmann, U Holland, et al.
Page
of 7