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S Garcia-Minaur

Showing results (1-10 of 11) with videos related to

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Clinical Dysmorphology|April 1, 1995
Setleis ('bitemporal forceps marks') syndromeS Garcia-Minaur, A Linares
American Journal of Medical Genetics|February 24, 2001
Further case of aminopterin syndrome sine aminopterin in a Spanish childS Garcia-Minaur, M P Botella
Clinical Dysmorphology|October 1, 1996
A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated familiesD Kumar, S Garcia-Minaur, O W Quarrell, et al.
Clinical Dysmorphology|July 12, 2001
Three new European cases of urofacial (Ochoa) syndromeS Garcia-Minaur, F Oliver, J M Yanez, et al.
Annales De Genetique|January 1, 1996
A study on limb reduction defects in six European regionsC Stoll, E Calzolari, M Cornel, et al.
British Journal of Cancer|January 8, 2004
A randomised controlled trial of a psychoeducational intervention for women at increased risk of breast cancerS Appleton, M Watson, R Rush, et al.
Journal of Medical Screening|February 24, 2001
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across EuropeP A Boyd, D G Wellesley, H E De Walle, et al.
Journal of Medical Genetics|February 5, 2008
Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardationR H Scott, J Douglas, L Baskcomb, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical Dysmorphology|April 1, 1995
Setleis ('bitemporal forceps marks') syndromeS Garcia-Minaur, A Linares
American Journal of Medical Genetics|February 24, 2001
Further case of aminopterin syndrome sine aminopterin in a Spanish childS Garcia-Minaur, M P Botella
Clinical Dysmorphology|October 1, 1996
A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated familiesD Kumar, S Garcia-Minaur, O W Quarrell, et al.
Clinical Dysmorphology|July 12, 2001
Three new European cases of urofacial (Ochoa) syndromeS Garcia-Minaur, F Oliver, J M Yanez, et al.
Annales De Genetique|January 1, 1996
A study on limb reduction defects in six European regionsC Stoll, E Calzolari, M Cornel, et al.
British Journal of Cancer|January 8, 2004
A randomised controlled trial of a psychoeducational intervention for women at increased risk of breast cancerS Appleton, M Watson, R Rush, et al.
Journal of Medical Screening|February 24, 2001
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across EuropeP A Boyd, D G Wellesley, H E De Walle, et al.
Journal of Medical Genetics|February 5, 2008
Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardationR H Scott, J Douglas, L Baskcomb, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.
Pageof 2