Category:Book:Handbook of Genetic Counseling
This category contains pages that are part of the Handbook of Genetic Counseling book. If a page of the book isn't showing here, please add text {{BookCat}} to the end of the page concerned. You can view a list of all subpages under the book main page (not including the book main page itself), regardless of whether they're categorized, here.
Pages in category "Book:Handbook of Genetic Counseling"
The following 200 pages are in this category, out of 205 total.
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A
- Handbook of Genetic Counseling/Abnormal Triple Screen and Family History of PKD
- Handbook of Genetic Counseling/Achondroplasia-1
- Handbook of Genetic Counseling/Achondroplasia-2
- Handbook of Genetic Counseling/Acrofacial Dysostosis Syndrome
- Handbook of Genetic Counseling/Advanced Maternal Age - Amniocentesis
- Handbook of Genetic Counseling/Advanced Maternal Age - Chorionic Villus Sampling (CVS)
- Handbook of Genetic Counseling/Advanced Maternal Age - Chorionic Villus Sampling (CVS)-2
- Handbook of Genetic Counseling/Advanced Maternal Age - Chorionic Villus Sampling (CVS)-3
- Handbook of Genetic Counseling/Allergies and Asthma
- Handbook of Genetic Counseling/Alpha 1 Antitrypsin Deficiency
- Handbook of Genetic Counseling/Alpha Thalassemia
- Handbook of Genetic Counseling/Alport Syndrome
- Handbook of Genetic Counseling/Amyotrophic Lateral Sclerosis
- Handbook of Genetic Counseling/Androgen Insensitivity Syndrome
- Handbook of Genetic Counseling/Anencephaly
- Handbook of Genetic Counseling/Angelman Syndrome-1
- Handbook of Genetic Counseling/Angelman Syndrome-2
- Handbook of Genetic Counseling/AR Sensorineural Hearing Loss (DFNB1/Connexin 26)
- Handbook of Genetic Counseling/Arthrogryposis
- Handbook of Genetic Counseling/Autism-1
- Handbook of Genetic Counseling/Autism-2
- Handbook of Genetic Counseling/Autism-3
B
- Handbook of Genetic Counseling/Balanced Robertsonian Translocation
- Handbook of Genetic Counseling/Balanced Translocation
- Handbook of Genetic Counseling/Bardet-Biedl Syndrome-1
- Handbook of Genetic Counseling/Bardet-Biedl Syndrome-2
- Handbook of Genetic Counseling/Beal's Syndrome
- Handbook of Genetic Counseling/Becker Muscular Dystrophy
- Handbook of Genetic Counseling/Beckwith-Wiedemann Syndrome
- Handbook of Genetic Counseling/Beta-Thalassemia
- Handbook of Genetic Counseling/Bloom Syndrome-1
- Handbook of Genetic Counseling/Bloom Syndrome-2
- Handbook of Genetic Counseling/Breast Cancer - Ashkenazi Jew
C
- Handbook of Genetic Counseling/CADASIL
- Handbook of Genetic Counseling/Canavan Disease: Heterozygote Screening
- Handbook of Genetic Counseling/Cancer
- Handbook of Genetic Counseling/Cerebral Palsy
- Handbook of Genetic Counseling/CHARGE Association
- Handbook of Genetic Counseling/Chondrodysplasia Punctata
- Handbook of Genetic Counseling/Chorionic Villus Sampling (CVS)
- Handbook of Genetic Counseling/Choroid Plexus Cysts on Ultrasound
- Handbook of Genetic Counseling/Classical Myotonic Dystrophy
- Handbook of Genetic Counseling/Cleft Lip - Isolated, Unilateral, Incomplete
- Handbook of Genetic Counseling/Cleft Lip and Palate
- Handbook of Genetic Counseling/Cleft Palate - Pierre Robin Sequence-1
- Handbook of Genetic Counseling/Cleft Palate - Pierre Robin Sequence-2
- Handbook of Genetic Counseling/Coeliac Disease
- Handbook of Genetic Counseling/Coffin-Lowry Syndrome
- Handbook of Genetic Counseling/Colon Cancer Prophylactic Surgery
- Handbook of Genetic Counseling/Colorectal Cancer Chemoprevention
- Handbook of Genetic Counseling/Congenital Diaphragmatic Hernia
- Handbook of Genetic Counseling/Cornelia de Lange Syndrome
- Handbook of Genetic Counseling/Counseling Methods
- Handbook of Genetic Counseling/Cowden Syndrome
- Handbook of Genetic Counseling/Craniosynostosis-1
- Handbook of Genetic Counseling/Craniosynostosis-2
- Handbook of Genetic Counseling/Cri-du-chat syndrome - deletion 5p
- Handbook of Genetic Counseling/Cystic Fibrosis - Prenatal Diagnosis-1
- Handbook of Genetic Counseling/Cystic Fibrosis - Prenatal Diagnosis-2
- Handbook of Genetic Counseling/Cystic Fibrosis Carrier Screening-1
- Handbook of Genetic Counseling/Cystic Fibrosis Carrier Screening-2
D
- Handbook of Genetic Counseling/Developmental Delay and Mental Retardation
- Handbook of Genetic Counseling/Developmental Delay and Mental Retardation-2
- Handbook of Genetic Counseling/Diabetes in Pregnancy
- Handbook of Genetic Counseling/Diabetes Mellitus
- Handbook of Genetic Counseling/Diabetic Embryopathy
- Handbook of Genetic Counseling/Down Syndrome - Trisomy 21-1
- Handbook of Genetic Counseling/Down Syndrome - Trisomy 21-2
- Handbook of Genetic Counseling/Duchenne Muscular Dystrophy-1
- Handbook of Genetic Counseling/Duchenne Muscular Dystrophy-2
- Handbook of Genetic Counseling/Dysmorphic Features - Developmental Delay
- Handbook of Genetic Counseling/Dysmorphic Features - Hypotonia
E
- Handbook of Genetic Counseling/Echogenic Bowel
- Handbook of Genetic Counseling/Ehlers-Danlos Syndrome
- Handbook of Genetic Counseling/Ehlers-Danlos Syndrome-2
- Handbook of Genetic Counseling/Ehlers-Danlos Syndrome-3
- Handbook of Genetic Counseling/Epilepsy and Seizures
- Handbook of Genetic Counseling/Ewing's Sarcoma
F
- Handbook of Genetic Counseling/Fabry Disease
- Handbook of Genetic Counseling/Familial Adenomatous Polyposis
- Handbook of Genetic Counseling/Familial Adenomatous Polyposis-2
- Handbook of Genetic Counseling/Fanconi Anemia
- Handbook of Genetic Counseling/Fetal Alcohol Syndrome
- Handbook of Genetic Counseling/Fetal Dilantin-Keppra Syndrome
- Handbook of Genetic Counseling/Fetal Hydantoin Syndrome
- Handbook of Genetic Counseling/Fetal Valproate Syndrome
- Handbook of Genetic Counseling/FG Syndrome
- Handbook of Genetic Counseling/FG Syndrome-2
- Handbook of Genetic Counseling/First Trimester Screening
- Handbook of Genetic Counseling/FISH
- Handbook of Genetic Counseling/Fragile X Syndrome
- Handbook of Genetic Counseling/Friedreich Ataxia
- Handbook of Genetic Counseling/Frontonasal Dysplasia - Median Cleft Face Syndrome
G
- Handbook of Genetic Counseling/Galactosemia
- Handbook of Genetic Counseling/Galactosemia-2
- Handbook of Genetic Counseling/Gastroschisis
- Handbook of Genetic Counseling/Gaucher Disease
- Handbook of Genetic Counseling/Gaucher Disease-2
- Handbook of Genetic Counseling/Gaucher Disease-3
- Handbook of Genetic Counseling/Genes and Chromosomes
- Handbook of Genetic Counseling/Gorlin - Nevoid Basal Cell Carcinoma Syndrome
H
- Handbook of Genetic Counseling/Hearing loss - Unknown Cause
- Handbook of Genetic Counseling/Heart Defects - Isolated
- Handbook of Genetic Counseling/Hemifacial Microsomia
- Handbook of Genetic Counseling/Hemoglobin C
- Handbook of Genetic Counseling/Hemoglobinopathy Screening and Hemoglobin D-Punjab
- Handbook of Genetic Counseling/Hemophilia and Von Willebrand Disease
- Handbook of Genetic Counseling/Hereditary Breast Cancer - BRCA1 and BRCA2
- Handbook of Genetic Counseling/Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) and Lobular Carcinoma In Situ (LCIS)
- Handbook of Genetic Counseling/Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
- Handbook of Genetic Counseling/HIgA Nephropathy
- Handbook of Genetic Counseling/Holoprosencephaly
- Handbook of Genetic Counseling/Huntington Disease
- Handbook of Genetic Counseling/Hyper-extensibility
- Handbook of Genetic Counseling/Hypoplasia - Agenesis of the Corpus Callosum
- Handbook of Genetic Counseling/Hypotonia - Developmental Delay
L
M
- Handbook of Genetic Counseling/Marfan Syndrome
- Handbook of Genetic Counseling/Maternal Serum Triple Screen
- Handbook of Genetic Counseling/Maternal Serum Triple Screen-2
- Handbook of Genetic Counseling/McCune Albright Syndrome
- Handbook of Genetic Counseling/Medium-chain acyl-coenzyme A dehydrogenase Deficiency
- Handbook of Genetic Counseling/Microcephaly
- Handbook of Genetic Counseling/Miller Syndrome
- Handbook of Genetic Counseling/Mosaic trisomy 21 - Transient Myeloproliferative Syndrome
- Handbook of Genetic Counseling/Mucopolysacharidosis (MPS)
- Handbook of Genetic Counseling/Multiple Pregnancy Loss
N
- Handbook of Genetic Counseling/Nager Syndrome
- Handbook of Genetic Counseling/Neural Tube Defects
- Handbook of Genetic Counseling/Neurofibromatosis - Type 1
- Handbook of Genetic Counseling/Neurofibromatosis - Type 1-2
- Handbook of Genetic Counseling/Neurofibromatosis - Type 1-3
- Handbook of Genetic Counseling/Neurofibromatosis - Type 2
- Handbook of Genetic Counseling/Niemann-Pick Disease
- Handbook of Genetic Counseling/Niemann-Pick Disease-2
- Handbook of Genetic Counseling/Noonan Syndrome
O
- Handbook of Genetic Counseling/Oculo-Auriculo-Vertebral Spectrum
- Handbook of Genetic Counseling/Opitz BBB - G Syndrome
- Handbook of Genetic Counseling/Oral-Facial-Digital Syndrome - Type 1
- Handbook of Genetic Counseling/Osteogenesis Imperfecta (OI)
- Handbook of Genetic Counseling/Osteosarcoma and Li-Fraumeni Syndrome
- Handbook of Genetic Counseling/Ovarian Cancer
P
- Handbook of Genetic Counseling/Pallister-Killian Syndrome
- Handbook of Genetic Counseling/Pancreatic Cancer
- Handbook of Genetic Counseling/Partial Trisomy 11q (q14-q21)
- Handbook of Genetic Counseling/Percutaneous Umbilical Blood Sampling (PUBS)
- Handbook of Genetic Counseling/Phenylketonuria (PKU)
- Handbook of Genetic Counseling/Pierre Robin Sequence - Cleft Palate
- Handbook of Genetic Counseling/Pituitary Tumor
- Handbook of Genetic Counseling/Polycystic Kidney Disease
- Handbook of Genetic Counseling/Polydactyly and Syndactyly
- Handbook of Genetic Counseling/Prader-Willi Syndrome - Prenatal
- Handbook of Genetic Counseling/Prader-Willi Syndrome-2
- Handbook of Genetic Counseling/Protein S Deficiency
R
- Handbook of Genetic Counseling/Reciprocal Translocation
- Handbook of Genetic Counseling/Renal Cell Carcinoma
- Handbook of Genetic Counseling/Retinoblastoma
- Handbook of Genetic Counseling/Rett Syndrome
- Handbook of Genetic Counseling/Ring Chromosome 22
- Handbook of Genetic Counseling/Robin Sequence
- Handbook of Genetic Counseling/Russell Silver Syndrome
S
- Handbook of Genetic Counseling/Sanfilippo syndrome
- Handbook of Genetic Counseling/Scheie Syndrome
- Handbook of Genetic Counseling/Seizure Medications
- Handbook of Genetic Counseling/Septo-optic dysplasia
- Handbook of Genetic Counseling/Short Chain Acyl-CoA Dehydrogenase (SCAD)
- Handbook of Genetic Counseling/Short Stature
- Handbook of Genetic Counseling/Sickle Cell Anemia
- Handbook of Genetic Counseling/Smith Magenis Syndrome
- Handbook of Genetic Counseling/Smith-Lemli-Opitz Syndrome
- Handbook of Genetic Counseling/Sotos Syndrome
- Handbook of Genetic Counseling/Spina Bifida
- Handbook of Genetic Counseling/Spinal Muscular Atrophy (SMA1)
- Handbook of Genetic Counseling/Spontaneous Pregnancy Loss and X-chromosome Inactivation
- Handbook of Genetic Counseling/Stickler Syndrome
T
- Handbook of Genetic Counseling/Tamoxifen - Selective Estrogen Response Modifiers (SERMS)
- Handbook of Genetic Counseling/Tay-Sachs Disease
- Handbook of Genetic Counseling/Treacher Collins
- Handbook of Genetic Counseling/Trisomy 13
- Handbook of Genetic Counseling/Trisomy 13 - Advanced Maternal Age - Occupational Exposures
- Handbook of Genetic Counseling/Trisomy 18
- Handbook of Genetic Counseling/Tuberous Sclerosis
- Handbook of Genetic Counseling/Tuberous Sclerosis-2
- Handbook of Genetic Counseling/Turner Syndrome
- Handbook of Genetic Counseling/Turner Syndrome-2