Search research articles
Contact Us
Filters
Showing results (21-30 of 47) with videos related to
Page
of 5
Sort By:
Clinical Genetics
|
April 1, 1985
Familial clefting syndrome with ectropion and dental anomaly--without limb anomalies
J E Allanson, B C McGillivray
Journal of Medical Genetics
|
October 1, 1989
Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives
M Pearson, C Riske, J E Allanson
Journal of Medical Genetics
|
June 3, 1999
The face of Smith-Magenis syndrome: a subjective and objective study
J E Allanson, F Greenberg, A C Smith
Journal of Medical Genetics
|
August 1, 1997
De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes
J E Allanson, R C Hennekam, M Ireland
American Journal of Medical Genetics
|
September 1, 1983
Possible new autosomal recessive syndrome with unusual renal histopathological changes
J E Allanson, J T Pantzar, P M MacLeod
American Journal of Medical Genetics
|
April 6, 2000
Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromes
R E Ward, P L Jamison, J E Allanson
Journal of Medical Genetics
|
December 1, 1998
Classical lissencephaly syndromes: does the face reflect the brain?
J E Allanson, D H Ledbetter, W B Dobyns
American Journal of Medical Genetics
|
July 1, 1985
Noonan phenotype associated with neurofibromatosis
J E Allanson, J G Hall, M I Van Allen
American Journal of Medical Genetics
|
July 15, 1992
Renal tubular dysgenesis: a not uncommon autosomal recessive syndrome: a review
J E Allanson, A G Hunter, G S Mettler, et al.
American Journal of Medical Genetics
|
October 1, 1993
Anthropometric craniofacial pattern profiles in Down syndrome
J E Allanson, P O'Hara, L G Farkas, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Clinical Genetics
|
April 1, 1985
Familial clefting syndrome with ectropion and dental anomaly--without limb anomalies
J E Allanson, B C McGillivray
Journal of Medical Genetics
|
October 1, 1989
Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives
M Pearson, C Riske, J E Allanson
Journal of Medical Genetics
|
June 3, 1999
The face of Smith-Magenis syndrome: a subjective and objective study
J E Allanson, F Greenberg, A C Smith
Journal of Medical Genetics
|
August 1, 1997
De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes
J E Allanson, R C Hennekam, M Ireland
American Journal of Medical Genetics
|
September 1, 1983
Possible new autosomal recessive syndrome with unusual renal histopathological changes
J E Allanson, J T Pantzar, P M MacLeod
American Journal of Medical Genetics
|
April 6, 2000
Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromes
R E Ward, P L Jamison, J E Allanson
Journal of Medical Genetics
|
December 1, 1998
Classical lissencephaly syndromes: does the face reflect the brain?
J E Allanson, D H Ledbetter, W B Dobyns
American Journal of Medical Genetics
|
July 1, 1985
Noonan phenotype associated with neurofibromatosis
J E Allanson, J G Hall, M I Van Allen
American Journal of Medical Genetics
|
July 15, 1992
Renal tubular dysgenesis: a not uncommon autosomal recessive syndrome: a review
J E Allanson, A G Hunter, G S Mettler, et al.
American Journal of Medical Genetics
|
October 1, 1993
Anthropometric craniofacial pattern profiles in Down syndrome
J E Allanson, P O'Hara, L G Farkas, et al.
Page
of 5