Journal of Medical Genetics

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Journal of Medical Genetics Journal

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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond-Blackfan anaemia. 47:777-781. 2010
THALASSEMIA IN AZERBAIJAN. 31:209-212. 1994
ANAPHASE LAG AS THE MOST LIKELY MECHANISM FOR MONOSOMY-X IN DIRECT CYTOTROPHOBLASTS BUT NOT IN MESENCHYMAL CORE CELLS FROM THE SAME VILLI. 27:780-781. 1990
OUTCOME AFTER PRENATAL DETECTION OF A SPORADIC, UNSTABLE TRANSLOCATION TERT(5-21). 23:274-278. 1986
HYPOSTATIC ULCERS IN 47,XXY KLINEFELTERS-SYNDROME. 20:100-101. 1983
CHRONIC RENAL-DISEASE, MYOTONIC-DYSTROPHY, AND GONADOBLASTOMA IN XY GONADAL-DYSGENESIS. 19:73-76. 1982
WEYERS ULNAR RAY OLIGODACTYLY SYNDROME AND THE ASSOCIATION OF MIDLINE MALFORMATIONS WITH ULNAR RAY DEFECTS 1992
3 DIFFERENT, NON-MOSAIC SEX-CHROMOSOME ABNORMALITIES (DIRECT CYTOTROPHOBLASTS, MESENCHYMAL CORE CULTURES, AND ABORTUS SKIN FIBROBLASTS) - IMPLICATIONS FOR ELUCIDATING CHORIONIC VILLI MOSAICISM 1989

International Standard Serial Number (ISSN)

0022-2593

Electronic International Standard Serial Number (EISSN)

1468-6244