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Journal of Medical Genetics
|
April 1, 1983
De novo tandem duplication 17p11 leads to cen
Z Docherty, M A Hultén, M M Honeyman
Clinical Dysmorphology
|
January 1, 1994
A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome
M J Seller, K Pal, Z Docherty, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach
H Hanson, C G Mathew, Z Docherty, et al.
American Journal of Medical Genetics
|
February 25, 2000
Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium
C M Ogilvie, J Moore, M Daker, et al.
Clinical Genetics
|
January 1, 1997
Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation
F Behjati, M Mullarkey, A Bergbaum, et al.
Clinical Dysmorphology
|
January 1, 1997
Phenotypic diversity in the Smith-Lemli-Opitz syndrome
M J Seller, F A Flinter, Z Docherty, et al.
Journal of Medical Genetics
|
December 10, 1997
Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique
C Mackie-Ogilvie, K Waddle, J Mandeville, et al.
Journal of Medical Genetics
|
April 16, 1998
A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome
C M Ogilvie, F L Raymond, R H Harrison, et al.
American Journal of Medical Genetics
|
July 14, 2000
Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31
P Warburton, G Baird, W Chen, et al.
Journal of Medical Genetics
|
June 1, 1993
Deletion 9p and sex reversal
C P Bennett, Z Docherty, S A Robb, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Journal of Medical Genetics
|
April 1, 1983
De novo tandem duplication 17p11 leads to cen
Z Docherty, M A Hultén, M M Honeyman
Clinical Dysmorphology
|
January 1, 1994
A fetus with an abnormal chromosome 7 and possible hydrolethalus syndrome
M J Seller, K Pal, Z Docherty, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach
H Hanson, C G Mathew, Z Docherty, et al.
American Journal of Medical Genetics
|
February 25, 2000
Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium
C M Ogilvie, J Moore, M Daker, et al.
Clinical Genetics
|
January 1, 1997
Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation
F Behjati, M Mullarkey, A Bergbaum, et al.
Clinical Dysmorphology
|
January 1, 1997
Phenotypic diversity in the Smith-Lemli-Opitz syndrome
M J Seller, F A Flinter, Z Docherty, et al.
Journal of Medical Genetics
|
December 10, 1997
Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique
C Mackie-Ogilvie, K Waddle, J Mandeville, et al.
Journal of Medical Genetics
|
April 16, 1998
A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome
C M Ogilvie, F L Raymond, R H Harrison, et al.
American Journal of Medical Genetics
|
July 14, 2000
Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31
P Warburton, G Baird, W Chen, et al.
Journal of Medical Genetics
|
June 1, 1993
Deletion 9p and sex reversal
C P Bennett, Z Docherty, S A Robb, et al.
Page
of 3