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P Meinecke

Showing results (71-80 of 93) with videos related to

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Clinical Dysmorphology|April 1, 1992
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese casesN Philip, P Meinecke, A David, et al.
Clinical Dysmorphology|May 8, 1998
The cerebro-costo-mandibular syndrome: seven patients and review of the literatureJ J van den Ende, C Schrander-Stumpel, E Rupprecht, et al.
Nature Genetics|June 1, 1993
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1N Tommerup, W Schempp, P Meinecke, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Cerebro-costo-mandibular syndrome: a follow-up study with 6 patientsC Schrander-Stumpel, S van der Meer, C De Die-Smulders, et al.
Clinical Genetics|August 6, 2011
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC geneR Nagy, H Wang, B Albrecht, et al.
European Journal of Pediatrics|June 1, 1994
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patientsC Schrander-Stumpel, P Meinecke, G Wilson, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
American Journal of Medical Genetics|September 6, 1996
Isochromosome Xq in Klinefelter syndrome: report of 7 new casesS Arps, T Koske-Westphal, P Meinecke, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Clinical Dysmorphology|April 1, 1992
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese casesN Philip, P Meinecke, A David, et al.
Clinical Dysmorphology|May 8, 1998
The cerebro-costo-mandibular syndrome: seven patients and review of the literatureJ J van den Ende, C Schrander-Stumpel, E Rupprecht, et al.
Nature Genetics|June 1, 1993
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1N Tommerup, W Schempp, P Meinecke, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Cerebro-costo-mandibular syndrome: a follow-up study with 6 patientsC Schrander-Stumpel, S van der Meer, C De Die-Smulders, et al.
Clinical Genetics|August 6, 2011
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC geneR Nagy, H Wang, B Albrecht, et al.
European Journal of Pediatrics|June 1, 1994
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patientsC Schrander-Stumpel, P Meinecke, G Wilson, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
American Journal of Medical Genetics|September 6, 1996
Isochromosome Xq in Klinefelter syndrome: report of 7 new casesS Arps, T Koske-Westphal, P Meinecke, et al.
American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.
Pageof 10