1,039 results on '"Ferguson-Smith, M"'
Search Results
52. Abnormalities of human sex determination
53. Disruption of the neuronal PAS3 gene in a family affected with schizophrenia
54. Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination
55. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation
56. Chromosome evolution in kangaroos (Marsupialia: Macropodidae): Cross species chromosome painting between the tammar wallaby and rock wallaby spp. with the 2n = 22 ancestral macropodid karyotype
57. Chromosome Analysis Before Birth And Its Value In Genetic Counselling
58. Multifaktorielle Vererbung
59. Anlage einer Genkarte
60. Geschlechtsgebundene Vererbung
61. Chromosomale Aberrationen
62. Autosomale Vererbung
63. Chromosomen
64. Gametogenese
65. Geschichte und Perspektiven der Humangenetik
66. Physiologische Grundlagen der Vererbung
67. Prävention und Behandlung genetischer Erkrankungen
68. Screeninguntersuchungen der Bevölkerung
69. Prävention und Therapie genetisch bedingter Erkrankungen: Pränatale Diagnostik
70. Kongenitale Mißbildungen
71. Molekularpathologie des Menschen
72. Multifaktoriell determinierte Erkrankungen
73. Durch ein Gen determinierte Krankheiten
74. Genetische Beratung
75. Immungenetik
76. Populationsgenetik
77. Reconstruction of the diapsid ancestral genome permits chromosome evolution tracing in avian and non-avian dinosaurs
78. Spina Bifida And Anencephaly
79. Genes On The X And Y Chromosomes Controlling Sex: Genetic Sex Is A Matter Of Quantity
80. Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21
81. Nature's Transplant
82. Chromosome Breakage And Ultrasound
83. The Triple-X Syndrome: Clinical, Pathological, And Chromosomal Studies In Three Mentally Retarded Cases
84. Research On Mental Defectives
85. Chromosomal Aberrations in Developmental Disease and Their Familial Transmission
86. Essential medical genetics: Fourth edition
87. Gestational experience alters sex allocation in the subsequent generation
88. New insights into sex chromosome evolution in anole lizards (Reptilia, Dactyloidae)
89. Paternal sex allocation: how variable is the sperm sex ratio?
90. The 11q;22q translocation: A European collaborative analysis of 43 cases
91. The chromosomal distribution of repetitive DNA sequences within the human β globin gene cluster
92. The potential of family flow karyotyping for the detection of chromosome abnormalities
93. Quantitative variation in cystic fibrosis-associated proteins in cystic fibrosis patients, carriers, and controls
94. Optimising human chromosome separation for the production of chromosome-specific DNA libraries by flow sorting
95. Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34
96. Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy
97. Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?
98. X Chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis)
99. Gene diagnosis in X-linked ichthyosis
100. Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome
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