Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
American Journal of Medical Genetics
|
May 1, 1991
Familial dermographism
K B Jedele, V V Michels
American Journal of Medical Genetics
|
July 1, 1990
Frequency of congenital heart defects in patients with hemophilia
K B Jedele, V V Michels, H Gordon, et al.
Pediatrics
|
May 1, 1992
Velo-cardio-facial syndrome associated with ventricular septal defect, pulmonary atresia, and hypoplastic pulmonary arteries
K B Jedele, V V Michels, F J Puga, et al.
Pediatrics
|
November 14, 1997
Large intergenerational variation in age of onset in two young patients with Huntington's disease presenting as dyskinesia
E Holinski-Feder, K B Jedele, K Hörtnagel, et al.
American Journal of Human Genetics
|
November 1, 1996
FRAXE testing
E Holinski-Feder, S Chahrokh-Zadeh, K B Jedele, et al.
American Journal of Medical Genetics
|
April 1, 1992
Linkage of nonspecific X-linked mental retardation to Xq21.31
K B Jedele, V V Michels, D J Schaid, et al.
Clinical Genetics
|
October 7, 1998
Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues
K B Jedele, D Wahl, S Chahrokh-Zadeh, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2
O Brandau, G Nyakatura, K B Jedele, et al.
American Journal of Medical Genetics
|
August 17, 1999
Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region
E Holinski-Feder, S Chahrockh-Zadeh, O Rittinger, et al.
Clinical Genetics
|
November 1, 1996
Discordant monozygotic twins with the Schimmelpenning-Feuerstein-Mims syndrome
H D Schworm, K B Jedele, E Holinski, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics
|
May 1, 1991
Familial dermographism
K B Jedele, V V Michels
American Journal of Medical Genetics
|
July 1, 1990
Frequency of congenital heart defects in patients with hemophilia
K B Jedele, V V Michels, H Gordon, et al.
Pediatrics
|
May 1, 1992
Velo-cardio-facial syndrome associated with ventricular septal defect, pulmonary atresia, and hypoplastic pulmonary arteries
K B Jedele, V V Michels, F J Puga, et al.
Pediatrics
|
November 14, 1997
Large intergenerational variation in age of onset in two young patients with Huntington's disease presenting as dyskinesia
E Holinski-Feder, K B Jedele, K Hörtnagel, et al.
American Journal of Human Genetics
|
November 1, 1996
FRAXE testing
E Holinski-Feder, S Chahrokh-Zadeh, K B Jedele, et al.
American Journal of Medical Genetics
|
April 1, 1992
Linkage of nonspecific X-linked mental retardation to Xq21.31
K B Jedele, V V Michels, D J Schaid, et al.
Clinical Genetics
|
October 7, 1998
Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues
K B Jedele, D Wahl, S Chahrokh-Zadeh, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2
O Brandau, G Nyakatura, K B Jedele, et al.
American Journal of Medical Genetics
|
August 17, 1999
Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region
E Holinski-Feder, S Chahrockh-Zadeh, O Rittinger, et al.
Clinical Genetics
|
November 1, 1996
Discordant monozygotic twins with the Schimmelpenning-Feuerstein-Mims syndrome
H D Schworm, K B Jedele, E Holinski, et al.
Page
of 2