Authors:
SLAVOTINEK A
ROSENBERG M
KNIGHT S
FERGUSSON W
GAUNT L
CLAYTONSMITH J
KINGSTON H
FLINT J
BIESECKER L
DONNAI D
Citation: A. Slavotinek et al., THE DETECTION OF SUBMICROSCOPIC CHROMOSOME REARRANGEMENTS IN CHILDRENWITH IDIOPATHIC MENTAL-RETARDATION AND PHYSICAL DIFFERENCES, European journal of human genetics, 6, 1998, pp. 2079-2079
Citation: A. Slavotinek et al., PATERNALLY INHERITED DUPLICATIONS OF 11P15.5 AND BECKWITH-WIEDEMANN-SYNDROME, Journal of Medical Genetics, 34(10), 1997, pp. 819-826
Authors:
SLAVOTINEK A
KNIGHT SJL
TASSABEHJI M
CLAYTONSMITH J
KINGSTON H
GAUNT L
FLINT J
DONNAI D
Citation: A. Slavotinek et al., SCREENING FOR SUBTELOMERIC CHROMOSOME DELETIONS IN CHILDREN WITH IDIOPATHIC MENTAL-RETARDATION, Journal of Medical Genetics, 34, 1997, pp. 1206-1206
Citation: J. Robinson et al., A CASE OF MOSAIC TRISOMY-2 DIAGNOSED AT AMNIOCENTESIS IN AN ABNORMAL FETUS AND CONFIRMED IN MULTIPLE FETAL TISSUES, Clinical genetics, 51(6), 1997, pp. 417-420
Authors:
MCGAUGHRAN JM
GAUNT L
DORE J
PETRIJ F
DAUWERSE HG
DONNAI D
Citation: Jm. Mcgaughran et al., RUBINSTEIN-TAYBI SYNDROME WITH DELETIONS OF FISH PROBE RT1 AT 16P13.3- 2 UK PATIENTS, Journal of Medical Genetics, 33(1), 1996, pp. 82-83
Citation: Ab. Dodge et al., PRENATAL EXCLUSION TEST OF A WOLF-HIRSCHHORN FAMILY USING PCR AMPLIFICATION WITH HUNTINGTONS-DISEASE PRIMERS, Journal of Medical Genetics, 32(2), 1995, pp. 149-149
Authors:
CLAYTONSMITH J
RAMSDEN SC
GAUNT L
SERESSANTAMARIA A
Citation: J. Claytonsmith et al., A CASE OF ANGELMAN-SYNDROME ARISING AS A RESULT OF A DE-NOVO ROBERTSONIAN 15 15-TRANSLOCATION/, Journal of Medical Genetics, 32(2), 1995, pp. 154-154
Authors:
WATSON CJ
GAUNT L
EVANS G
PATEL K
HARRIS R
STRACHAN T
Citation: Cj. Watson et al., A DISEASE-ASSOCIATED GERMLINE DELETION MAPS THE TYPE-2 NEUROFIBROMATOSIS (NF2) GENE BETWEEN THE EWING SARCOMA REGION AND THE LEUKEMIA INHIBITORY FACTOR LOCUS, Human molecular genetics, 2(6), 1993, pp. 701-704