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American Journal of Medical Genetics
|
July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child
J L Tolmie, M McNay, J B Stephenson, et al.
Prenatal Diagnosis
|
October 1, 1987
Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism
J L Tolmie, M E Ferguson-Smith, D Gilmore, et al.
Human Genetics
|
January 1, 1990
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination
M A Ferguson-Smith, A Cooke, N A Affara, et al.
Clinical Dysmorphology
|
January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)
P D Turnpenny, R Davidson, E J Stockdale, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Hurler-Scheie phenotype associated with consanguinity
D L Davies, G N Dutton, J Farquharson, et al.
American Journal of Medical Genetics
|
May 1, 1987
The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sib
J L Tolmie, G Mortimer, D Doyle, et al.
Journal of Medical Genetics
|
October 23, 1998
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation
S R Ghaffari, E Boyd, J M Connor, et al.
Human Genetics
|
August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry
A Cooke, J L Tolmie, J M Colgan, et al.
Clinical Dysmorphology
|
April 20, 2001
A new case of Myhre syndrome
M L Whiteford, W B Doig, P A Raine, et al.
Journal of Medical Genetics
|
March 1, 1996
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study
E Reid, N Morrison, L Barron, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 72) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics
|
July 1, 1987
Microcephaly: genetic counselling and antenatal diagnosis after the birth of an affected child
J L Tolmie, M McNay, J B Stephenson, et al.
Prenatal Diagnosis
|
October 1, 1987
Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism
J L Tolmie, M E Ferguson-Smith, D Gilmore, et al.
Human Genetics
|
January 1, 1990
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination
M A Ferguson-Smith, A Cooke, N A Affara, et al.
Clinical Dysmorphology
|
January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)
P D Turnpenny, R Davidson, E J Stockdale, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Hurler-Scheie phenotype associated with consanguinity
D L Davies, G N Dutton, J Farquharson, et al.
American Journal of Medical Genetics
|
May 1, 1987
The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sib
J L Tolmie, G Mortimer, D Doyle, et al.
Journal of Medical Genetics
|
October 23, 1998
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation
S R Ghaffari, E Boyd, J M Connor, et al.
Human Genetics
|
August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry
A Cooke, J L Tolmie, J M Colgan, et al.
Clinical Dysmorphology
|
April 20, 2001
A new case of Myhre syndrome
M L Whiteford, W B Doig, P A Raine, et al.
Journal of Medical Genetics
|
March 1, 1996
Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study
E Reid, N Morrison, L Barron, et al.
Page
of 8