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Archives of Disease in Childhood
|
July 1, 1991
Cleft lip--is there light at the end of the tunnel?
S E Holder
Journal of Medical Genetics
|
April 1, 1993
Otopalatodigital syndrome type II
S E Holder, R M Winter
Clinical and Experimental Dermatology
|
January 8, 2019
The protean manifestations of RASA1 gene mutation
P Nicholson, S E Holder, J Carton, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 16, 2003
Isolated non-compaction of the ventricular myocardium: prenatal diagnosis and natural history
A A Karatza, S E Holder, H M Gardiner
The Journal of Laryngology and Otology
|
December 20, 2005
Chondrodysplasia punctata: case report and review of audiological and ENT features
L Murdin, T Sirimanna, B E Hartley, et al.
The British Journal of Dermatology
|
July 15, 2018
Uniparental disomy as a mechanism for CERS3-mutated autosomal recessive congenital ichthyosis
S Polubothu, M Glover, S E Holder, et al.
Journal of Medical Genetics
|
October 1, 1993
Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype
S E Holder, R M Winter, S Kamath, et al.
Journal of Medical Genetics
|
June 1, 1992
No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate
G M Vintiner, S E Holder, R M Winter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 19, 2003
Skeletal muscle involvement in infantile systemic hyalinosis
Zarazuela Zolkipli, Cheryl Longman, Sue Brown, et al.
Journal of Medical Genetics
|
June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate
S E Holder, G M Vintiner, B Farren, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Archives of Disease in Childhood
|
July 1, 1991
Cleft lip--is there light at the end of the tunnel?
S E Holder
Journal of Medical Genetics
|
April 1, 1993
Otopalatodigital syndrome type II
S E Holder, R M Winter
Clinical and Experimental Dermatology
|
January 8, 2019
The protean manifestations of RASA1 gene mutation
P Nicholson, S E Holder, J Carton, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
January 16, 2003
Isolated non-compaction of the ventricular myocardium: prenatal diagnosis and natural history
A A Karatza, S E Holder, H M Gardiner
The Journal of Laryngology and Otology
|
December 20, 2005
Chondrodysplasia punctata: case report and review of audiological and ENT features
L Murdin, T Sirimanna, B E Hartley, et al.
The British Journal of Dermatology
|
July 15, 2018
Uniparental disomy as a mechanism for CERS3-mutated autosomal recessive congenital ichthyosis
S Polubothu, M Glover, S E Holder, et al.
Journal of Medical Genetics
|
October 1, 1993
Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype
S E Holder, R M Winter, S Kamath, et al.
Journal of Medical Genetics
|
June 1, 1992
No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate
G M Vintiner, S E Holder, R M Winter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 19, 2003
Skeletal muscle involvement in infantile systemic hyalinosis
Zarazuela Zolkipli, Cheryl Longman, Sue Brown, et al.
Journal of Medical Genetics
|
June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palate
S E Holder, G M Vintiner, B Farren, et al.
Page
of 2