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J A Crolla

Showing results (51-60 of 78) with videos related to

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American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.
Journal of Medical Genetics|November 14, 1997
Isolated sacral agenesis in a fetus monosomic for 7q36.1-->qterN M Savage, N A Maclachlan, C A Joyce, et al.
Journal of Medical Genetics|June 4, 1998
Triplication of 15q11-q13 with inv dup(15) in a female with developmental delayF L Long, D P Duckett, L J Billam, et al.
Journal of Medical Genetics|July 5, 2003
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotypeF Maggouta, S E Roberts, N R Dennis, et al.
British Journal of Cancer|January 10, 2013
Male breast cancer, age and sex chromosome aneuploidyP A Jacobs, V Maloney, R Cooke, et al.
Journal of Medical Genetics|June 1, 1993
Three patients with ring (X) chromosomes and a severe phenotypeN R Dennis, A L Collins, J A Crolla, et al.
Cytogenetic and Genome Research|May 24, 2006
A highly complex rea(2;3;11) and aniridia by position effectH Rivera, M L Ayala-Madrigal, J P Barros-Núñez, et al.
Prenatal Diagnosis|April 1, 1996
A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9T A Wilkinson, R S James, J A Crolla, et al.
Journal of Medical Genetics|May 5, 1999
A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndromeD O Robinson, P Dalton, P A Jacobs, et al.
Cytogenetic and Genome Research|November 9, 2005
Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalitiesA E Cockwell, V K Maloney, N S Thomas, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|March 1, 1986
A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndromeS V Hodgson, J Z Heckmatt, E Hughes, et al.
Journal of Medical Genetics|November 14, 1997
Isolated sacral agenesis in a fetus monosomic for 7q36.1-->qterN M Savage, N A Maclachlan, C A Joyce, et al.
Journal of Medical Genetics|June 4, 1998
Triplication of 15q11-q13 with inv dup(15) in a female with developmental delayF L Long, D P Duckett, L J Billam, et al.
Journal of Medical Genetics|July 5, 2003
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotypeF Maggouta, S E Roberts, N R Dennis, et al.
British Journal of Cancer|January 10, 2013
Male breast cancer, age and sex chromosome aneuploidyP A Jacobs, V Maloney, R Cooke, et al.
Journal of Medical Genetics|June 1, 1993
Three patients with ring (X) chromosomes and a severe phenotypeN R Dennis, A L Collins, J A Crolla, et al.
Cytogenetic and Genome Research|May 24, 2006
A highly complex rea(2;3;11) and aniridia by position effectH Rivera, M L Ayala-Madrigal, J P Barros-Núñez, et al.
Prenatal Diagnosis|April 1, 1996
A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9T A Wilkinson, R S James, J A Crolla, et al.
Journal of Medical Genetics|May 5, 1999
A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndromeD O Robinson, P Dalton, P A Jacobs, et al.
Cytogenetic and Genome Research|November 9, 2005
Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalitiesA E Cockwell, V K Maloney, N S Thomas, et al.
Pageof 8