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American Journal of Medical Genetics
|
February 2, 1996
Fibrodysplasia ossificans progressiva in two half-sisters: evidence for maternal mosaicism
H B Janoff, M Muenke, L O Johnson, et al.
Plastic and Reconstructive Surgery
|
December 18, 2001
Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary report
L B Cassileth, S P Bartlett, P M Glat, et al.
Genomics
|
January 20, 1995
The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21
G T Berry, J J Mallee, H M Kwon, et al.
American Journal of Medical Genetics
|
December 30, 1996
Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?
R L Kelley, E Roessler, R C Hennekam, et al.
Human Genetics
|
August 2, 2001
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly
I M Orioli, E E Castilla, J E Ming, et al.
Lancet (London, England)
|
April 12, 1997
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis
D M Moloney, S A Wall, G J Ashworth, et al.
The Journal of Rheumatology
|
May 1, 1995
Mild expression of fibrodysplasia ossificans progressiva: a report of 3 cases
H B Janoff, J A Tabas, E M Shore, et al.
BMC Medical Genomics
|
May 10, 2018
A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature
C S Paththinige, N D Sirisena, U G I U Kariyawasam, et al.
American Journal of Human Genetics
|
February 1, 1991
In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA
V Montanaro, A Casamassimi, M D'Urso, et al.
European Journal of Biochemistry
|
May 12, 2000
ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells
P Jay, J L Bergé-Lefranc, A Massacrier, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 104) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
February 2, 1996
Fibrodysplasia ossificans progressiva in two half-sisters: evidence for maternal mosaicism
H B Janoff, M Muenke, L O Johnson, et al.
Plastic and Reconstructive Surgery
|
December 18, 2001
Clinical characteristics of patients with unicoronal synostosis and mutations of fibroblast growth factor receptor 3: a preliminary report
L B Cassileth, S P Bartlett, P M Glat, et al.
Genomics
|
January 20, 1995
The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21
G T Berry, J J Mallee, H M Kwon, et al.
American Journal of Medical Genetics
|
December 30, 1996
Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?
R L Kelley, E Roessler, R C Hennekam, et al.
Human Genetics
|
August 2, 2001
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly
I M Orioli, E E Castilla, J E Ming, et al.
Lancet (London, England)
|
April 12, 1997
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis
D M Moloney, S A Wall, G J Ashworth, et al.
The Journal of Rheumatology
|
May 1, 1995
Mild expression of fibrodysplasia ossificans progressiva: a report of 3 cases
H B Janoff, J A Tabas, E M Shore, et al.
BMC Medical Genomics
|
May 10, 2018
A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature
C S Paththinige, N D Sirisena, U G I U Kariyawasam, et al.
American Journal of Human Genetics
|
February 1, 1991
In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA
V Montanaro, A Casamassimi, M D'Urso, et al.
European Journal of Biochemistry
|
May 12, 2000
ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells
P Jay, J L Bergé-Lefranc, A Massacrier, et al.
Page
of 11