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Atlas of Genetic Diagnosis and Counseling

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Cover of 'Atlas of Genetic Diagnosis and Counseling'

Table of Contents

  1. Altmetric Badge
    Book Overview
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    Chapter 1 Acardia
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    Chapter 2 Achondrogenesis
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    Chapter 3 Achondroplasia
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    Chapter 4 Adams-Oliver Syndrome
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    Chapter 5 Agnathia
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    Chapter 6 Aicardi Syndrome
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    Chapter 7 Alagille Syndrome
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    Chapter 8 Albinism
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    Chapter 9 Amniotic Band Syndrome
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    Chapter 10 Androgen Insensitivity Syndrome
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    Chapter 11 Angelman Syndrome
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    Chapter 12 Apert Syndrome
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    Chapter 13 Aplasia Cutis Congenita
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    Chapter 14 Arthrogryposis Multiplex Congenita
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    Chapter 15 Asphyxiating Thoracic Dystrophy
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    Chapter 16 Ataxia Telangiectasia
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    Chapter 17 Atelosteogenesis
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    Chapter 18 Autism
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    Chapter 19 Beckwith-Wiedemann Syndrome
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    Chapter 20 Behcet Disease
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    Chapter 21 Bladder Exstrophy
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    Chapter 22 Body Stalk Anomaly
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    Chapter 23 Branchial Cleft Anomalies
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    Chapter 24 Campomelic Dysplasia
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    Chapter 25 Cat Eye Syndrome
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    Chapter 26 Cerebro-Costo-Mandibular Syndrome
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    Chapter 27 Charcot-Marie-Tooth Disease
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    Chapter 28 CHARGE Association
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    Chapter 29 Cherubism
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    Chapter 30 Chiari Malformation
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    Chapter 31 Chondrodysplasia Punctata
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    Chapter 32 Chromosome Abnormalities in Pediatric Solid Tumors
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    Chapter 33 Cleft Lip and/or Cleft Palate
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    Chapter 34 Cleidocranial Dysplasia
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    Chapter 35 Cloacal Exstrophy
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    Chapter 36 Collodion Baby
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    Chapter 37 Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)
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    Chapter 38 Congenital Cutis Laxa
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    Chapter 39 Congenital Cytomegalovirus Infection
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    Chapter 40 Congenital Generalized Lipodystrophy
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    Chapter 41 Congenital Hydrocephalus
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    Chapter 42 Congenital Hypothyroidism
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    Chapter 43 Congenital Muscular Dystrophy
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    Chapter 44 Congenital Toxoplasmosis
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    Chapter 45 Conjoined Twins
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    Chapter 46 Corpus Callosum Agenesis/Dysgenesis
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    Chapter 47 Craniometaphyseal Dysplasia
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    Chapter 48 Cri-Du-Chat Syndrome
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    Chapter 49 Crouzon Syndrome
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    Chapter 50 Cystic Fibrosis
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    Chapter 51 Dandy-Walker Malformation
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    Chapter 52 De Lange Syndrome
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    Chapter 53 Del(22q11.2) Syndromes
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    Chapter 54 Diabetic Embryopathy
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    Chapter 55 Down Syndrome
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    Chapter 56 Dyschondrosteosis (Leri-Weill Syndrome) and Langer Mesomelic Dysplasia
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    Chapter 57 Dysmelia (Limb Deficiency/Reduction)
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    Chapter 58 Dysplasia Epiphysealis Hemimelica
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    Chapter 59 Dystonia
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    Chapter 60 Dystrophinopathies
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    Chapter 61 Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome
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    Chapter 62 Ehlers-Danlos Syndrome
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    Chapter 63 Ellis-van Creveld Syndrome
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    Chapter 64 Enchondromatosis (Maffucci Syndrome; Ollier Syndrome)
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    Chapter 65 Epidermolysis Bullosa
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    Chapter 66 Epidermolytic Palmoplantar Keratoderma
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    Chapter 67 Faciogenital (Aarskog) Dysplasia
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    Chapter 68 Facioscapulohumeral Muscular Dystrophy
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    Chapter 69 Familial Adenomatous Polyposis
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    Chapter 70 Familial Hyperlysinemia
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    Chapter 71 Fanconi Anemia
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    Chapter 72 Femoral Hypoplasia-Unusual Facies Syndrome
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    Chapter 73 Fetal Akinesia Sequence
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    Chapter 74 Fetal Alcohol Syndrome
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    Chapter 75 Fetal Hydantoin Syndrome
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    Chapter 76 Fibrodysplasia Ossificans Progressiva
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    Chapter 77 Finlay-Marks Syndrome
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    Chapter 78 Fragile X Syndrome
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    Chapter 79 Fraser Syndrome
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    Chapter 80 Freeman-Sheldon Syndrome
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    Chapter 81 Frontonasal Dysplasia
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    Chapter 82 Galactosemia
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    Chapter 83 Gastroschisis
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    Chapter 84 Gaucher Disease
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    Chapter 85 Generalized Arterial Calcification of Infancy
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    Chapter 86 Glucose-6-Phosphate Dehydrogenase Deficiency
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    Chapter 87 Glycogen Storage Disease, Type II
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    Chapter 88 Goldenhar Syndrome
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    Chapter 89 Hallermann-Streiff Syndrome
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    Chapter 90 Harlequin Ichthyosis (Harlequin Fetus)
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    Chapter 91 Hemophilia A
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    Chapter 92 Hereditary Hemochromatosis
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    Chapter 93 Hereditary Multiple Exostoses
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    Chapter 94 Holoprosencephaly
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    Chapter 95 Holt-Oram Syndrome
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    Chapter 96 Hydrops Fetalis
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    Chapter 97 Hyper-IgE Syndrome
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    Chapter 98 Hypochondroplasia
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    Chapter 99 Hypoglossia-Hypodactylia Syndrome
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    Chapter 100 Hypohidrotic Ectodermal Dysplasia
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    Chapter 101 Hypomelanosis of Ito
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    Chapter 102 Hypophosphatasia
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    Chapter 103 Incontinentia Pigmenti
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    Chapter 104 Infantile Myofibromatosis
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    Chapter 105 Ivemark Syndrome
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    Chapter 106 Jarcho-Levin Syndrome
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    Chapter 107 Kabuki Syndrome
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    Chapter 108 Kasabach-Merritt Syndrome
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    Chapter 109 KID Syndrome
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    Chapter 110 Klinefelter Syndrome
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    Chapter 111 Klippel-Feil Syndrome
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    Chapter 112 Klippel-Trenaunay Syndrome
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    Chapter 113 Kniest Dysplasia
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    Chapter 114 Larsen Syndrome
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    Chapter 115 LEOPARD Syndrome
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    Chapter 116 Lesch-Nyhan Syndrome
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    Chapter 117 Lethal Multiple Pterygium Syndrome
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    Chapter 118 Lowe Syndrome
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    Chapter 119 Marfan Syndrome
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    Chapter 120 McCune-Albright Syndrome
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    Chapter 121 Meckel-Gruber Syndrome
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    Chapter 122 Menkes Disease (Kinky-Hair Syndrome)
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    Chapter 123 Metachromatic Leukodystrophy
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    Chapter 124 Miller-Dieker Syndrome
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    Chapter 125 Möbius Syndrome
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    Chapter 126 Mucolipidosis II (I-Cell Disease)
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    Chapter 127 Mucolipidosis III (Pseudo-Hurler Polydystrophy)
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    Chapter 128 Mucopolysaccharidosis I (MPS I) (α- L -Iduronidase Deficiency): Hurler (MPS I-H), Hurler-Scheie (MPS I-H/S), and Scheie (MPS I-S) Syndromes
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    Chapter 129 Mucopolysaccharidosis II (Hunter Syndrome)
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    Chapter 130 Mucopolysaccharidosis III (Sanfilippo Syndrome)
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    Chapter 131 Mucopolysaccharidosis IV (Morquio Syndrome)
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    Chapter 132 Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)
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    Chapter 133 Multiple Epiphyseal Dysplasia
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    Chapter 134 Multiple Pterygium Syndrome
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    Chapter 135 Myotonic Dystrophy Type I
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    Chapter 136 Netherton Syndrome
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    Chapter 137 Neu-Laxova Syndrome
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    Chapter 138 Neural Tube Defects
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    Chapter 139 Neurofibromatosis I
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    Chapter 140 Noonan Syndrome
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    Chapter 141 Oblique Facial Cleft Syndrome
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    Chapter 142 Oligohydramnios Sequence
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    Chapter 143 Omphalocele
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    Chapter 144 Osteogenesis Imperfecta
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    Chapter 145 Osteopetrosis
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    Chapter 146 Pachyonychia Congenita
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    Chapter 147 Pallister-Killian Syndrome
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    Chapter 148 Phenylketonuria (PKU)
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    Chapter 149 Pierre Robin Sequence
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    Chapter 150 Polycystic Kidney Disease, Autosomal Dominant Type
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    Chapter 151 Polycystic Kidney Disease, Autosomal Recessive Type
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    Chapter 152 Prader-Willi Syndrome
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    Chapter 153 Progeria
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    Chapter 154 Prune Belly Syndrome
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    Chapter 155 Pseudoachondroplasia
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    Chapter 156 R(18) Syndrome
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    Chapter 157 Retinoid Embryopathy
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    Chapter 158 Rett Syndrome
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    Chapter 159 Rickets
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    Chapter 160 Roberts Syndrome
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    Chapter 161 Robinow Syndrome
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    Chapter 162 Rubinstein-Taybi Syndrome
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    Chapter 163 Schizencephaly
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    Chapter 164 Schmid Metaphyseal Chondrodysplasia
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    Chapter 165 Seckel Syndrome
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    Chapter 166 Severe Combined Immune Deficiency
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    Chapter 167 Short Rib Polydactyly Syndromes
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    Chapter 168 Sickle Cell Disease
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    Chapter 169 Silver-Russell Syndrome
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    Chapter 170 Sirenomelia
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    Chapter 171 Smith-Lemli-Opitz Syndrome
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    Chapter 172 Smith-Magenis Syndrome
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    Chapter 173 Sotos Syndrome
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    Chapter 174 Spinal Muscular Atrophy
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    Chapter 175 Spondyloepiphyseal Dysplasia
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    Chapter 176 Stickler Syndrome
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    Chapter 177 Sturge-Weber Syndrome
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    Chapter 178 Tay-Sachs Disease
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    Chapter 179 Tetrasomy 9p Syndrome
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    Chapter 180 Thalassemia
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    Chapter 181 Thanatophoric Dysplasia
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    Chapter 182 Thrombocytopenia-Absent Radius Syndrome
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    Chapter 183 Treacher-Collins Syndrome
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    Chapter 184 Trimethylaminuria
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    Chapter 185 Triploidy
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    Chapter 186 Trismus Pseudocamptodactyly Syndrome
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    Chapter 187 Trisomy 13 Syndrome
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    Chapter 188 Trisomy 18 Syndrome
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    Chapter 189 Tuberous Sclerosis
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    Chapter 190 Turner Syndrome
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    Chapter 191 Twin-Twin Transfusion Syndrome
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    Chapter 192 Ulnar-Mammary Syndrome
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    Chapter 193 VATER (VACTERL) Association
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    Chapter 194 Von Hippel-Lindau Disease
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    Chapter 195 Waardenburg Syndrome
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    Chapter 196 Williams Syndrome
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    Chapter 197 Wolf-Hirschhorn Syndrome
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    Chapter 198 X-Linked Ichthyosis
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    Chapter 199 XXX Syndrome
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    Chapter 200 XXXXX Syndrome
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    Chapter 201 XXXXY Syndrome
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    Chapter 202 XY Female
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    Chapter 203 XYY Syndrome
Attention for Chapter 179: Tetrasomy 9p Syndrome
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Chapter title
Tetrasomy 9p Syndrome
Chapter number 179
Book title
Atlas of Genetic Diagnosis and Counseling
Published by
Humana Press, December 2015
DOI 10.1007/978-1-60327-161-5_179
Book ISBNs
978-1-58829-681-8, 978-1-60327-161-5
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 17%
Unknown 5 83%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 33%
Librarian 1 17%
Professor > Associate Professor 1 17%
Student > Postgraduate 1 17%
Unknown 1 17%
Readers by discipline Count As %
Medicine and Dentistry 4 67%
Biochemistry, Genetics and Molecular Biology 1 17%
Unknown 1 17%