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Journal of Medical Genetics
|
September 1, 1992
The acrocallosal syndrome and Greig syndrome are not allelic disorders
L A Brueton, K A Chotai, L van Herwerden, et al.
Archives of Disease in Childhood
|
July 1, 1988
Pulmonary agenesis as part of the VACTERL sequence
S Knowles, R M Thomas, R H Lindenbaum, et al.
Clinical Dysmorphology
|
October 1, 1996
Extreme intrauterine growth retardation, hydrocephalus and aged facial appearance: a previously unrecognized autosomal recessive disorder?
R M Winter, D Shortland, A L Collins, et al.
Journal of Medical Genetics
|
September 1, 1993
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies
G M Vintiner, K K Lo, S E Holder, et al.
Clinical Dysmorphology
|
April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiae
M Baraitser, F Stewart, R M Winter, et al.
Clinical Dysmorphology
|
April 1, 1996
An unusual presentation of Smith-Magenis syndrome with iris dysgenesis
A J Barnicoat, H U Moller, R W Palmer, et al.
Nature Genetics
|
September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
W Reardon, R M Winter, P Rutland, et al.
Clinical Dysmorphology
|
April 1, 1994
A case with blepharophimosis resembling Ohdo syndrome
J A Maat-Kievit, P J Milla, J E Collins, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Clinical Dysmorphology
|
May 29, 2000
Radial aplasia, poikiloderma and auto-immune enterocolitis--new syndrome or severe form of Rothmund-Thomson syndrome?
Y Hilhorst-Hofstee, N Shah, D Atherton, et al.
Page
of 22
Search research articles
Search
Showing results (151-160 of 219) with videos related to
Sort By:
Page
of 22
Journal of Medical Genetics
|
September 1, 1992
The acrocallosal syndrome and Greig syndrome are not allelic disorders
L A Brueton, K A Chotai, L van Herwerden, et al.
Archives of Disease in Childhood
|
July 1, 1988
Pulmonary agenesis as part of the VACTERL sequence
S Knowles, R M Thomas, R H Lindenbaum, et al.
Clinical Dysmorphology
|
October 1, 1996
Extreme intrauterine growth retardation, hydrocephalus and aged facial appearance: a previously unrecognized autosomal recessive disorder?
R M Winter, D Shortland, A L Collins, et al.
Journal of Medical Genetics
|
September 1, 1993
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies
G M Vintiner, K K Lo, S E Holder, et al.
Clinical Dysmorphology
|
April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiae
M Baraitser, F Stewart, R M Winter, et al.
Clinical Dysmorphology
|
April 1, 1996
An unusual presentation of Smith-Magenis syndrome with iris dysgenesis
A J Barnicoat, H U Moller, R W Palmer, et al.
Nature Genetics
|
September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
W Reardon, R M Winter, P Rutland, et al.
Clinical Dysmorphology
|
April 1, 1994
A case with blepharophimosis resembling Ohdo syndrome
J A Maat-Kievit, P J Milla, J E Collins, et al.
Human Genetics
|
July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisation
R M Winter, K E Davies, M V Bell, et al.
Clinical Dysmorphology
|
May 29, 2000
Radial aplasia, poikiloderma and auto-immune enterocolitis--new syndrome or severe form of Rothmund-Thomson syndrome?
Y Hilhorst-Hofstee, N Shah, D Atherton, et al.
Page
of 22