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I Kennerknecht

Showing results (1-10 of 44) with videos related to

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Clinical Genetics|March 1, 1989
Prader-Willi syndrome and Sotos syndromeI Kennerknecht
Human Genetics|September 1, 1992
A genetic model for the Prader-Willi syndrome and its implication for Angelman syndromeI Kennerknecht
Clinical Genetics|June 1, 1992
Differentiated recurrence risk estimations in the Prader-Willi syndromeI Kennerknecht
Prenatal Diagnosis|August 1, 1990
Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: triple trisomy 6,21,22; trisomy 16; and trisomy 18I Kennerknecht, R Terinde
American Journal of Medical Genetics|December 1, 1993
Dup(1q)(q42-->qter) syndrome: case report and review of literatureI Kennerknecht, G Barbi, K Rodens
Ophthalmic Genetics|March 1, 1994
Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13qI Kennerknecht, G Barbi, J Greher
Prenatal Diagnosis|September 1, 1993
A triploid fetus with a diploid placenta: proposal of a mechanismI Kennerknecht, W Just, W Vogel
Prenatal Diagnosis|December 1, 1993
A modified embryogenic model to explain embryonic/extraembryonic chromosomal inconsistenciesI Kennerknecht, W Vogel, K Mehnert
Genomics|October 1, 1992
Assignment of the human gene propionyl coenzyme A carboxylase, alpha-chain, (PCCA) to chromosome 13q32 by in situ hybridizationI Kennerknecht, C Klett, H Hameister
American Journal of Medical Genetics|July 1, 1992
Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)G Barbi, I Kennerknecht, C Klett
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Clinical Genetics|March 1, 1989
Prader-Willi syndrome and Sotos syndromeI Kennerknecht
Human Genetics|September 1, 1992
A genetic model for the Prader-Willi syndrome and its implication for Angelman syndromeI Kennerknecht
Clinical Genetics|June 1, 1992
Differentiated recurrence risk estimations in the Prader-Willi syndromeI Kennerknecht
Prenatal Diagnosis|August 1, 1990
Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: triple trisomy 6,21,22; trisomy 16; and trisomy 18I Kennerknecht, R Terinde
American Journal of Medical Genetics|December 1, 1993
Dup(1q)(q42-->qter) syndrome: case report and review of literatureI Kennerknecht, G Barbi, K Rodens
Ophthalmic Genetics|March 1, 1994
Diagnosis of retinoblastoma in a presymptomatic stage after detection of interstitial chromosomal deletion 13qI Kennerknecht, G Barbi, J Greher
Prenatal Diagnosis|September 1, 1993
A triploid fetus with a diploid placenta: proposal of a mechanismI Kennerknecht, W Just, W Vogel
Prenatal Diagnosis|December 1, 1993
A modified embryogenic model to explain embryonic/extraembryonic chromosomal inconsistenciesI Kennerknecht, W Vogel, K Mehnert
Genomics|October 1, 1992
Assignment of the human gene propionyl coenzyme A carboxylase, alpha-chain, (PCCA) to chromosome 13q32 by in situ hybridizationI Kennerknecht, C Klett, H Hameister
American Journal of Medical Genetics|July 1, 1992
Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)G Barbi, I Kennerknecht, C Klett
Pageof 5