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R H Lindenbaum

Showing results (1-10 of 56) with videos related to

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Human Genetics|June 1, 1990
Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis IR H Lindenbaum
Journal of Medical Genetics|March 1, 1975
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspringR H Lindenbaum, M Bobrow
Archives of Disease in Childhood|August 1, 1981
Benign (non-paroxysmal) familial chorea. Paediatric perspectivesG Sleigh, R H Lindenbaum
Journal of Medical Genetics|August 1, 1984
Tuberous sclerosis: a new estimate of prevalence within the Oxford regionA Hunt, R H Lindenbaum
The British Journal of Psychiatry : the Journal of Mental Science|October 1, 1990
Prevalence of Huntington's disease among UK immigrants from the Indian subcontinentR S Shiwach, R H Lindenbaum
Archives of Disease in Childhood|February 1, 1971
Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-)R H Lindenbaum, L J Butler
Clinical Genetics|October 1, 1987
Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relativesN A Lygidakis, R H Lindenbaum
Journal of Medical Genetics|January 1, 1992
UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disordersH V Firth, R H Lindenbaum
Oral Surgery, Oral Medicine, and Oral Pathology|December 1, 1989
Oral fibromatosis in tuberous sclerosisN A Lygidakis, R H Lindenbaum
Journal of Medical Genetics|March 1, 1973
Monozygotic twins with ring chromosome 22R H Lindenbaum, M Bobrow, L Barber
Pageof 6

Showing results (1-10 of 56) with videos related to

Sort By:
Pageof 6
Human Genetics|June 1, 1990
Unusual segregation of constitutional 11q;22q translocation may be explained by crossover in interchange segment, followed by 3:1 segregation at meiosis IR H Lindenbaum
Journal of Medical Genetics|March 1, 1975
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspringR H Lindenbaum, M Bobrow
Archives of Disease in Childhood|August 1, 1981
Benign (non-paroxysmal) familial chorea. Paediatric perspectivesG Sleigh, R H Lindenbaum
Journal of Medical Genetics|August 1, 1984
Tuberous sclerosis: a new estimate of prevalence within the Oxford regionA Hunt, R H Lindenbaum
The British Journal of Psychiatry : the Journal of Mental Science|October 1, 1990
Prevalence of Huntington's disease among UK immigrants from the Indian subcontinentR S Shiwach, R H Lindenbaum
Archives of Disease in Childhood|February 1, 1971
Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-)R H Lindenbaum, L J Butler
Clinical Genetics|October 1, 1987
Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relativesN A Lygidakis, R H Lindenbaum
Journal of Medical Genetics|January 1, 1992
UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disordersH V Firth, R H Lindenbaum
Oral Surgery, Oral Medicine, and Oral Pathology|December 1, 1989
Oral fibromatosis in tuberous sclerosisN A Lygidakis, R H Lindenbaum
Journal of Medical Genetics|March 1, 1973
Monozygotic twins with ring chromosome 22R H Lindenbaum, M Bobrow, L Barber
Pageof 6