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Prenatal Diagnosis
|
January 12, 2002
Duplication of chromosome 2 in association with ventriculomegaly - a case report
W L Martin, S Pretlove, A Mercer, et al.
Journal of Clinical Pathology
|
November 1, 1987
Cytogenic investigations in the assessment of response to treatment in neuroblastoma
N Bown, M M Reid, A D Pearson, et al.
Medical and Pediatric Oncology
|
January 1, 1994
Cytogenetic abnormalities of small round cell tumours
N P Bown, M M Reid, A J Malcolm, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis
S C Hillman, S Pretlove, A Coomarasamy, et al.
Medical and Pediatric Oncology
|
January 1, 1993
Cytogenetic abnormalities in a disseminated medulloblastoma
A G Stuart, A D Pearson, J Emslie, et al.
Journal of Psychoactive Drugs
|
January 1, 1982
A clinical guide to the diagnosis and treatment of heroin-related sexual dysfunction
D E Smith, C Moser, D R Wesson, et al.
Prenatal Diagnosis
|
November 1, 1996
Structural chromosome anomalies in congenital diaphragmatic hernia
D T Howe, M D Kilby, H Sirry, et al.
European Journal of Cancer (Oxford, England : 1990)
|
May 15, 2007
Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population
A Ng, A Griffiths, T Cole, et al.
Journal of Medical Genetics
|
July 1, 1992
Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13)
A S Goldman, R H Martin, R Johannisson, et al.
Human Genetics
|
December 22, 1998
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1
N Rahman, F Abidi, D Ford, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
Prenatal Diagnosis
|
January 12, 2002
Duplication of chromosome 2 in association with ventriculomegaly - a case report
W L Martin, S Pretlove, A Mercer, et al.
Journal of Clinical Pathology
|
November 1, 1987
Cytogenic investigations in the assessment of response to treatment in neuroblastoma
N Bown, M M Reid, A D Pearson, et al.
Medical and Pediatric Oncology
|
January 1, 1994
Cytogenetic abnormalities of small round cell tumours
N P Bown, M M Reid, A J Malcolm, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis
S C Hillman, S Pretlove, A Coomarasamy, et al.
Medical and Pediatric Oncology
|
January 1, 1993
Cytogenetic abnormalities in a disseminated medulloblastoma
A G Stuart, A D Pearson, J Emslie, et al.
Journal of Psychoactive Drugs
|
January 1, 1982
A clinical guide to the diagnosis and treatment of heroin-related sexual dysfunction
D E Smith, C Moser, D R Wesson, et al.
Prenatal Diagnosis
|
November 1, 1996
Structural chromosome anomalies in congenital diaphragmatic hernia
D T Howe, M D Kilby, H Sirry, et al.
European Journal of Cancer (Oxford, England : 1990)
|
May 15, 2007
Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population
A Ng, A Griffiths, T Cole, et al.
Journal of Medical Genetics
|
July 1, 1992
Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13)
A S Goldman, R H Martin, R Johannisson, et al.
Human Genetics
|
December 22, 1998
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1
N Rahman, F Abidi, D Ford, et al.
Page
of 5