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Clinical Genetics
|
September 1, 1979
Five familial cases with a trisomy 16p syndrome due to translocation
N J Leschot, J J De Nef, J P Geraedts, et al.
Journal of Medical Genetics
|
April 1, 1979
Two cases with different deletions of the long arm of chromosome 7
J M Klep-de Pater, J B Bijlsma, E M Bleeker-Wagemakers, et al.
Archives of Neurology
|
January 1, 1986
Familial association of intracranial aneurysms and multiple congenital anomalies
H W ter Berg, J B Bijlsma, J A Veiga Pires, et al.
American Journal of Medical Genetics. Part A
|
July 15, 2005
Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literature
M H de Ru, J J P Gille, A W M Nieuwint, et al.
Human Genetics
|
June 30, 1977
Localization of HLA on the short arm of chromosome 6
M H Breuning, E M van den Berg-Loonen, L F Bernini, et al.
Human Genetics
|
January 19, 1979
Partial trisomy 10q: a recognizable syndrome
J M Klep-de Pater, J B Bijlsma, H F de France, et al.
European Journal of Medical Genetics
|
February 14, 2006
Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18
J M de Pater, M Poot, F A Beemer, et al.
American Journal of Medical Genetics
|
June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes
A M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 38 results.
Clinical Genetics
|
September 1, 1979
Five familial cases with a trisomy 16p syndrome due to translocation
N J Leschot, J J De Nef, J P Geraedts, et al.
Journal of Medical Genetics
|
April 1, 1979
Two cases with different deletions of the long arm of chromosome 7
J M Klep-de Pater, J B Bijlsma, E M Bleeker-Wagemakers, et al.
Archives of Neurology
|
January 1, 1986
Familial association of intracranial aneurysms and multiple congenital anomalies
H W ter Berg, J B Bijlsma, J A Veiga Pires, et al.
American Journal of Medical Genetics. Part A
|
July 15, 2005
Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literature
M H de Ru, J J P Gille, A W M Nieuwint, et al.
Human Genetics
|
June 30, 1977
Localization of HLA on the short arm of chromosome 6
M H Breuning, E M van den Berg-Loonen, L F Bernini, et al.
Human Genetics
|
January 19, 1979
Partial trisomy 10q: a recognizable syndrome
J M Klep-de Pater, J B Bijlsma, H F de France, et al.
European Journal of Medical Genetics
|
February 14, 2006
Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18
J M de Pater, M Poot, F A Beemer, et al.
American Journal of Medical Genetics
|
June 27, 1997
The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes
A M Zwamborn-Hanssen, J B Bijlsma, E F Hennekam, et al.
Page
of 4