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M le Merrer

Showing results (121-130 of 188) with videos related to

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Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.
Human Genetics|March 1, 1997
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostosesL Legeai-Mallet, P Margaritte-Jeannin, M Lemdani, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 27, 2009
Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case reportA Benaicha, M Dommergues, J M Jouannic, et al.
Nature Genetics|May 1, 1995
Stop codon FGFR3 mutations in thanatophoric dwarfism type 1F Rousseau, P Saugier, M Le Merrer, et al.
Prenatal Diagnosis|January 24, 2007
Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic imagesM Sinico, J M Levaillant, A Vergnaud, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
Pageof 19

Showing results (121-130 of 188) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|October 1, 1994
OsteocraniostenosisA Verloes, F Narcy, B Grattagliano, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
Journal of Medical Genetics|January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeL Faivre, M Le Merrer, A Megarbane, et al.
Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.
European Journal of Medical Genetics|June 10, 2006
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate regionM Chaabouni, M Le Merrer, O Raoul, et al.
Human Genetics|March 1, 1997
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostosesL Legeai-Mallet, P Margaritte-Jeannin, M Lemdani, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 27, 2009
Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case reportA Benaicha, M Dommergues, J M Jouannic, et al.
Nature Genetics|May 1, 1995
Stop codon FGFR3 mutations in thanatophoric dwarfism type 1F Rousseau, P Saugier, M Le Merrer, et al.
Prenatal Diagnosis|January 24, 2007
Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic imagesM Sinico, J M Levaillant, A Vergnaud, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
Pageof 19