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V Shashi

Showing results (1-10 of 30) with videos related to

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Clinical Genetics|December 1, 1995
Vascular ring leading to tracheoesophageal compression in a patient with Rubinstein-Taybi syndromeV Shashi, J S Fryburg
American Journal of Medical Genetics|May 5, 2001
Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defectsV Shashi, A Rickheim, M J Pettenati
American Journal of Medical Genetics|January 1, 1994
Choanal atresia in a patient with the deletion (9p) syndromeV Shashi, W L Golden, J S Fryburg
The Journal of Urology|February 1, 1997
Water intoxication in a patient with the Prader-Willi syndrome treated with desmopressin for nocturnal enuresisW L Robson, V Shashi, S Nagaraj, et al.
American Journal of Medical Genetics|August 10, 1999
Partial duplication of 4q12q13 leads to a mild phenotypeV Shashi, M N Berry, C Santos, et al.
American Journal of Medical Genetics|May 22, 1995
Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS?V Shashi, P Clark, A D Rogol, et al.
Journal of Medical Genetics|June 1, 1995
Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported casesV Shashi, J Zunich, T E Kelly, et al.
American Journal of Medical Genetics|March 1, 1996
Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?V Shashi, W L Golden, C von Kap-Herr, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of complete sole trisomy 1qM J Pettenati, M Berry, V Shashi, et al.
Cancer Genetics and Cytogenetics|December 1, 1995
Loss of chromosomes 22 and 14 in the malignant progression of meningiomas. A comparative study of fluorescence in situ hybridization (FISH) and standard cytogenetic analysisB F Schneider, V Shashi, C von Kap-herr, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Clinical Genetics|December 1, 1995
Vascular ring leading to tracheoesophageal compression in a patient with Rubinstein-Taybi syndromeV Shashi, J S Fryburg
American Journal of Medical Genetics|May 5, 2001
Maternal homozygosity for the common MTHFR mutation as a potential risk factor for offspring with limb defectsV Shashi, A Rickheim, M J Pettenati
American Journal of Medical Genetics|January 1, 1994
Choanal atresia in a patient with the deletion (9p) syndromeV Shashi, W L Golden, J S Fryburg
The Journal of Urology|February 1, 1997
Water intoxication in a patient with the Prader-Willi syndrome treated with desmopressin for nocturnal enuresisW L Robson, V Shashi, S Nagaraj, et al.
American Journal of Medical Genetics|August 10, 1999
Partial duplication of 4q12q13 leads to a mild phenotypeV Shashi, M N Berry, C Santos, et al.
American Journal of Medical Genetics|May 22, 1995
Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS?V Shashi, P Clark, A D Rogol, et al.
Journal of Medical Genetics|June 1, 1995
Neuroectodermal (CHIME) syndrome: an additional case with long term follow up of all reported casesV Shashi, J Zunich, T E Kelly, et al.
American Journal of Medical Genetics|March 1, 1996
Constellation of congenital abnormalities in an infant: a new syndrome or tissue-specific mosaicism for trisomy 18?V Shashi, W L Golden, C von Kap-Herr, et al.
Prenatal Diagnosis|July 5, 2001
Prenatal diagnosis of complete sole trisomy 1qM J Pettenati, M Berry, V Shashi, et al.
Cancer Genetics and Cytogenetics|December 1, 1995
Loss of chromosomes 22 and 14 in the malignant progression of meningiomas. A comparative study of fluorescence in situ hybridization (FISH) and standard cytogenetic analysisB F Schneider, V Shashi, C von Kap-herr, et al.
Pageof 3