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T R Cole

Showing results (31-40 of 37) with videos related to

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Journal of Medical Genetics|May 1, 1992
Small cell lung carcinoma in a patient with Sotos syndrome: are genes at 3p21 involved in both conditions?T R Cole, H E Hughes, M J Jeffreys, et al.
American Journal of Medical Genetics|May 15, 1994
Metacarpophalangeal pattern profile analysis in Sotos and Marfan syndromeP F Dijkstra, T R Cole, J W Oorthuys, et al.
Journal of Medical Genetics|July 31, 2001
Chromosome 2 interstitial deletion (del(2)(q14.1q21)) associated with connective tissue laxity and an attention deficit disorderK L Baker, M I Rees, P W Thompson, et al.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Human Molecular Genetics|March 11, 1999
Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.
Journal of Medical Genetics|January 15, 2003
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)E R Maher, L A Brueton, S C Bowdin, 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.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Journal of Medical Genetics|May 1, 1992
Small cell lung carcinoma in a patient with Sotos syndrome: are genes at 3p21 involved in both conditions?T R Cole, H E Hughes, M J Jeffreys, et al.
American Journal of Medical Genetics|May 15, 1994
Metacarpophalangeal pattern profile analysis in Sotos and Marfan syndromeP F Dijkstra, T R Cole, J W Oorthuys, et al.
Journal of Medical Genetics|July 31, 2001
Chromosome 2 interstitial deletion (del(2)(q14.1q21)) associated with connective tissue laxity and an attention deficit disorderK L Baker, M I Rees, P W Thompson, et al.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Human Molecular Genetics|March 11, 1999
Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.
Journal of Medical Genetics|January 15, 2003
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)E R Maher, L A Brueton, S C Bowdin, 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.
Pageof 4