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M M Rinaldi

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Annales De Genetique|January 1, 1992
Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locusG Stoppoloni, M Stabile, M M Rinaldi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)]G Scarano, M M Rinaldi, M L Cavaliere, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1982
[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?]M M Rinaldi, R Militerni, A Pascotto, et al.
Ophthalmic Genetics|July 27, 1999
Retinal degeneration associated with ectopia lentisF Simonelli, G De Crecchio, F Testa, et al.
Clinical Genetics|July 25, 2000
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosisG Palka, L Stuppia, P Guanciali Franchi, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Clinical Genetics|November 27, 1998
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneityG de Crecchio, F Simonelli, G Nunziata, et al.
Journal of Medical Genetics|February 5, 2003
SHOX mutations detected by FISH and direct sequencing in patients with short statureL Stuppia, G Calabrese, V Gatta, et al.
Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Annales De Genetique|January 1, 1992
Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locusG Stoppoloni, M Stabile, M M Rinaldi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)]G Scarano, M M Rinaldi, M L Cavaliere, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1982
[Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?]M M Rinaldi, R Militerni, A Pascotto, et al.
Ophthalmic Genetics|July 27, 1999
Retinal degeneration associated with ectopia lentisF Simonelli, G De Crecchio, F Testa, et al.
Clinical Genetics|July 25, 2000
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosisG Palka, L Stuppia, P Guanciali Franchi, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Deletion of the SHOX gene in patients with short stature of unknown causeE Morizio, L Stuppia, V Gatta, et al.
Clinical Genetics|November 27, 1998
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneityG de Crecchio, F Simonelli, G Nunziata, et al.
Journal of Medical Genetics|February 5, 2003
SHOX mutations detected by FISH and direct sequencing in patients with short statureL Stuppia, G Calabrese, V Gatta, et al.
Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
Pageof 2