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Journal of Medical Genetics
|
September 1, 1991
Do familial neural tube defects breed true?
E Drainer, H M May, J L Tolmie
American Journal of Medical Genetics
|
October 1, 1989
Oliver McFarlane syndrome: a 25-year follow-up
J R Sampson, J L Tolmie, J S Cant
Journal of Medical Genetics
|
July 1, 1989
Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth
R C Shepherd, D R Goudie, J L Tolmie
Archives of Disease in Childhood
|
May 1, 1991
Genetic aspects of admissions to a paediatric intensive care unit
D R FitzPatrick, C H Skeoch, J L Tolmie
Clinical Genetics
|
June 1, 1986
Partial deletion of the short arm of chromosome 3
J L Tolmie, P Batstone, I Ruthven, et al.
Archives of Disease in Childhood
|
July 26, 2002
Cataplexy in the Prader-Willi syndrome
E S Tobias, J L Tolmie, J B P Stephenson
Clinical Dysmorphology
|
January 1, 1995
A cognitively normal boy with meningoencephalocele, arthrogryposis and hypoplastic thumbs
S Podder, R C Shepherd, P Shillito, et al.
Archives of Disease in Childhood
|
November 26, 1999
Towards earlier diagnosis of 22q11 deletions
E S Tobias, N Morrison, M L Whiteford, et al.
American Journal of Medical Genetics
|
September 1, 1988
Congenital diaphragmatic defects and maternal serum alphafetoprotein
J A Crossley, J L Tolmie, D A Aitken, et al.
Prenatal Diagnosis
|
April 1, 1994
Simpson-Golabi-Behmel syndrome: disproportionate fetal overgrowth and elevated maternal serum alpha-fetoprotein
R M Hughes-Benzie, J L Tolmie, M McNay, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 72) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
September 1, 1991
Do familial neural tube defects breed true?
E Drainer, H M May, J L Tolmie
American Journal of Medical Genetics
|
October 1, 1989
Oliver McFarlane syndrome: a 25-year follow-up
J R Sampson, J L Tolmie, J S Cant
Journal of Medical Genetics
|
July 1, 1989
Unknown syndrome: Noonan-like craniofacial features, digital anomalies, and premature birth
R C Shepherd, D R Goudie, J L Tolmie
Archives of Disease in Childhood
|
May 1, 1991
Genetic aspects of admissions to a paediatric intensive care unit
D R FitzPatrick, C H Skeoch, J L Tolmie
Clinical Genetics
|
June 1, 1986
Partial deletion of the short arm of chromosome 3
J L Tolmie, P Batstone, I Ruthven, et al.
Archives of Disease in Childhood
|
July 26, 2002
Cataplexy in the Prader-Willi syndrome
E S Tobias, J L Tolmie, J B P Stephenson
Clinical Dysmorphology
|
January 1, 1995
A cognitively normal boy with meningoencephalocele, arthrogryposis and hypoplastic thumbs
S Podder, R C Shepherd, P Shillito, et al.
Archives of Disease in Childhood
|
November 26, 1999
Towards earlier diagnosis of 22q11 deletions
E S Tobias, N Morrison, M L Whiteford, et al.
American Journal of Medical Genetics
|
September 1, 1988
Congenital diaphragmatic defects and maternal serum alphafetoprotein
J A Crossley, J L Tolmie, D A Aitken, et al.
Prenatal Diagnosis
|
April 1, 1994
Simpson-Golabi-Behmel syndrome: disproportionate fetal overgrowth and elevated maternal serum alpha-fetoprotein
R M Hughes-Benzie, J L Tolmie, M McNay, et al.
Page
of 8