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T J De Ravel

Showing results (11-20 of 21) with videos related to

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Prenatal Diagnosis|April 21, 1999
Hydrolethalus syndrome in a non-Finnish family: confirmation of the entity and early prenatal diagnosisT J de Ravel, M C van der Griendt, P Evan, et al.
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
The ICF syndrome: new case and updateT J De Ravel, E Deckers, P L Alliet, et al.
Physiological Measurement|November 1, 1993
Bandwidths of respiratory gas flow and pressure waveforms in mechanically ventilated infantsM J Turner, V A Davies, T J De Ravel, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 17, 1991
Non-ketotic hyperglycinaemia in a neonate. A case reportT J De Ravel, C E Smith, L G Scher, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
The Pallister-Killian syndrome in an African individualB F Woodman, M A Jordan, L I Moller, et al.
Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center studyJ D Cogan, B Ramel, M Lehto, et al.
Journal of Medical Genetics|September 1, 1996
First report of CFTR mutations in black cystic fibrosis patients of southern African originS Carles, M Desgeorges, A Goldman, et al.
Journal of Medical Genetics|November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia familiesR A Gibson, D Ford, S Jansen, et al.
Journal of Medical Genetics|September 13, 2005
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 geneM C J Jongmans, R J Admiraal, K P van der Donk, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|April 21, 1999
Hydrolethalus syndrome in a non-Finnish family: confirmation of the entity and early prenatal diagnosisT J de Ravel, M C van der Griendt, P Evan, et al.
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
The ICF syndrome: new case and updateT J De Ravel, E Deckers, P L Alliet, et al.
Physiological Measurement|November 1, 1993
Bandwidths of respiratory gas flow and pressure waveforms in mechanically ventilated infantsM J Turner, V A Davies, T J De Ravel, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 17, 1991
Non-ketotic hyperglycinaemia in a neonate. A case reportT J De Ravel, C E Smith, L G Scher, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
The Pallister-Killian syndrome in an African individualB F Woodman, M A Jordan, L I Moller, et al.
Clinical Dysmorphology|October 23, 2001
Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factorT J de Ravel, E Legius, H Brems, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center studyJ D Cogan, B Ramel, M Lehto, et al.
Journal of Medical Genetics|September 1, 1996
First report of CFTR mutations in black cystic fibrosis patients of southern African originS Carles, M Desgeorges, A Goldman, et al.
Journal of Medical Genetics|November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia familiesR A Gibson, D Ford, S Jansen, et al.
Journal of Medical Genetics|September 13, 2005
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 geneM C J Jongmans, R J Admiraal, K P van der Donk, et al.
Pageof 3