C. Moss

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A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

W. Reardon, R. Winter, S. Malcolm, 1996, Journal of medical genetics.

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

Julie C. Sapp, L. Biesecker, M. Topf, 2018, The Journal of clinical investigation.

0·03% tacrolimus ointment applied once or twice daily is more efficacious than 1% hydrocortisone acetate in children with moderate to severe atopic dermatitis: results of a randomized double‐blind controlled trial

C. Bruijnzeel-Koomen, S. Reitamo, F. Cambazard, 2004, The British journal of dermatology.

Rothmund–Thomson Syndrome, Bloom Syndrome, Dyskeratosis Congenita, Fanconi Anaemia

C. Moss, 2011 .

Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.

J. McGrath, J. Mellerio, Lu Liu, 2011, Acta dermato-venereologica.

EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype–phenotype correlation?

H. van Bokhoven, L. Adès, N. Graf, 2007, American journal of medical genetics. Part A.

Randomised controlled study of early pulsed dye laser treatment of uncomplicated childhood haemangiomas: results of a 1-year analysis

HywelC. Williams, L. Hiller, C. Moss, 2002, The Lancet.

Cytogenetic and molecular evidence for cutaneous mosaicism: the ectodermal origin of Blaschko lines.

C. Moss, 1999, American journal of medical genetics.

Revertant mosaicism in Kindler syndrome.

J. McGrath, M. Parsons, C. Moss, 2012, The Journal of investigative dermatology.

Gonosomal mosaicism for a nonsense mutation (R1947X) in the NF1 gene in segmental neurofibromatosis type 1.

D. Cooper, M. Upadhyaya, C. Moss, 2005, The Journal of investigative dermatology.

Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetrance

R. Desnick, L. Edelmann, D. Weaver, 2015, Journal of Human Genetics.

A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene.

H. Cox, S. Robins, P. Farndon, 2008, American journal of human genetics.

Osteogenic sarcoma in the Rothmund-Thomson syndrome.

A. Craft, A. Malcolm, C. Moss, 1996, Medical and pediatric oncology.

Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes

D. Bennett, C. Moss, S. Taibjee, 2004, The British journal of dermatology.

Type 2 segmental Cowden disease vs. Proteus syndrome: reply from authors

T. Cole, C. Moss, N. Mclellan, 2007, The British journal of dermatology.

Epidermal naevus in Proteus syndrome showing loss of heterozygosity for an inherited PTEN mutation

T. Cole, S. Payne, C. Moss, 2006, The British journal of dermatology.

Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis

G. Mortier, J. Hellemans, A. De Paepe, 2006, Human mutation.

Classification of aplasia cutis congenita: a 25‐year review of cases presenting to a tertiary paediatric dermatology department

C. Moss, M. Ogboli, D. Sathishkumar, 2020, Clinical and experimental dermatology.

A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis.

A. Christiano, A. Martinez-Mir, H. Lam, 2004, The Journal of investigative dermatology.

Quantitative relationships between sensitizing dose of DNCB and reactivity in normal subjects.

S. Shuster, P. Friedmann, J. Simpson, 1983, Clinical and experimental immunology.

The Desktop Guide to Complementary and Alternative Medicine: an Evidence-based Approach

C. Moss, 2001 .

RASopathies and the skin

C. Moss, 2019, The British journal of dermatology.

The 100 000 Genomes Project: feeding back to patients

A. Wernham, C. Moss, 2018, British Medical Journal.

Expression of 25‐hydroxyvitamin D3‐1α‐hydroxylase in subcutaneous fat necrosis

D. Zehnder, M. Hewison, N. Shaw, 2009, The British journal of dermatology.

Birthmark due to cutaneous mosaicism for keratin 10 mutation

A. Blight, C. Moss, P. Bowden, 1995, The Lancet.

A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

E. Lane, R. Eady, N. West, 2000, The British journal of dermatology.

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

J. McGrath, I. Leigh, R. Eady, 2004, The Journal of investigative dermatology.

Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex.

E. Lane, D. Hohl, I. Leigh, 1997, The Journal of investigative dermatology.

Two new XPD patients compound heterozygous for the same mutation demonstrate diverse clinical features.

H. Nakagawa, A. Lehmann, M. Momoi, 2005, The Journal of investigative dermatology.

Analysis of urinary cathepsin C for diagnosing Papillon – Lef (cid:1) evre syndrome

A. Vlahou, P. Fergelot, M. Battino, 2016 .

Early‐onset urticaria: a marker of cryopyrin‐associated periodic syndrome

P. Hawkins, C. Moss, E. Al-Abadi, 2017, Clinical and experimental dermatology.

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

C. Bodemer, J. Uitto, J. McGrath, 2020, The British journal of dermatology.

Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes

S. Larkins, C. Moss, S. Taibjee, 2009, Clinical and experimental dermatology.

Fibroblast growth factor receptor 3 (FGFR3) mutation in a verrucous epidermal naevus associated with mild facial dysmorphism

I. B. Taylor, B. Collin, C. Moss, 2007, The British journal of dermatology.

What is segmental neurofibromatosis?

S. Green, C. Moss, 1994, The British journal of dermatology.

Epidermal mosaicism and Blaschko's lines.

S. Larkins, M. Stacey, P. Farndon, 1993, Journal of medical genetics.

Bullous congenital ichthyosiform erythroderma clinically resembling neonatal staphylococcal scalded skin syndrome

N. Levell, C. Moss, C. Upton, 2009, Clinical and experimental dermatology.

Two families with Greither's syndrome caused by a keratin 1 mutation.

E. Lane, C. Munro, N. Wilson, 2005, Journal of the American Academy of Dermatology.

Guidelines for the diagnosis and management of individuals with neurofibromatosis 1

D. Evans, M. Gleeson, S. Huson, 2006, Journal of Medical Genetics.

individuals with Neurofibromatosis 1 (NF1) Guidelines for the diagnosis and management of

M. Gleeson, S. Huson, M. Upadhyaya, 2007 .

Antigenic stimulation during ultraviolet therapy in man does not result in immunological tolerance.

P. Friedmann, C. Moss, J. Matthews, 1989, Clinical and experimental immunology.

Early pulsed-dye laser treatment of childhood haemangiomas

HywelC. Williams, L. Hiller, C. Moss, 2003, The Lancet.

End-stage renal failure in adolescence with Sjögren’s syndrome autoantibodies SSA and SSB

S. Hulton, S. Johnson, M. Brundler, 2007, Pediatric Nephrology.

Familial progressive hyper‐ and hypopigmentation and malignancy in two families with new mutations in KITLG

J. McGrath, T. Cole, T. Takeichi, 2015, Clinical and experimental dermatology.

Pyogenic Skin Infections as a Presentation of Papillon-Lefèvre Syndrome: Phenotypic Variability or Under-Reporting?

I. Chapple, Liqun Zhang, C. Moss, 2005 .

Hereditary Vitamin D–Resistant Rickets Presenting as Alopecia

U. Kini, S. Burge, C. Moss, 2014, Pediatric dermatology.

INHIBITION OF DELAYED HYPERSENSITIVITY SKIN REACTIONS IN PATIENTS ON METHOXYPSORALEN PHOTOCHEMOTHERAPY

S. Shuster, C. Moss, P. Friedmann, 1980, The Lancet.

Compound heterozygous mutations in desmoplakin cause skin fragility and woolly hair

J. McGrath, N. Wilson, C. Moss, 2012, The British journal of dermatology.

CUTANEOUS REACTIONS TO ALUMINIUM IN VACCINES: AN AVOIDABLE PROBLEM

N. Cox, C. Moss, A. Forsyth, 1988, The Lancet.

Naevi and Other Developmental Defects

H. Shahidullah, C. Moss, 2008 .

Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases.

D. Kelsell, H. Kayserili, C. Mein, 2011, Archives of dermatology.

Development of a clinical diagnostic matrix for characterizing inherited epidermolysis bullosa

V. Sharma, V. Sreenivas, C. Moss, 2017, The British journal of dermatology.

Susceptibility and amplification of sensitivity in contact dermatitis.

S. Shuster, P. Friedmann, J. Simpson, 1985, Clinical and experimental immunology.

Contact urticaria to play dough: a possible sign of dietary allergy

C. Moss, S. Baron, 2003, The British journal of dermatology.

Rothmund‐Thomson syndrome: a report of two patients and a review of the literature

C. Moss, 1990, The British journal of dermatology.

Scalp ringworm epidemic in Birmingham: a decline?

D. Buckley, C. Moss, J. Leeming, 2000, Clinical and experimental dermatology.

X‐linked dyskeratosis congenita presenting in adulthood with photodamaged skin and epiphora

I. Dokal, B. Cave, R. Carr, 2014, Clinical and experimental dermatology.

‘Tinea indecisiva’ may mimic the concentric rings of tinea imbricata

A. Smith, C. Moss, D. Ramlogan, 2002, The British journal of dermatology.

Proactive disease management with 0·03% tacrolimus ointment for children with atopic dermatitis: results of a randomized, multicentre, comparative study

M. Sebastian, S. Reitamo, D. Thaçi, 2008, The British journal of dermatology.

Does gastrostomy benefit patients with epidermolysis bullosa? We need to collaborate to find out

C. Moss, 2018, The British journal of dermatology.

Macrocephaly-cutis marmorata telangiectatica congenita: A case report and review of salient features.

R. Katugampola, C. Mills, C. Moss, 2008, Journal of the American Academy of Dermatology.

Pityriasis rubra pilaris in a mother and two daughters

C. Moss, M. A. Thomson, M. Thomson, 2007, The British journal of dermatology.

Genetic skin disorders.

C. Moss, 2000, Seminars in neonatology : SN.

Precocious puberty in a boy with a widespread linear epidermal naevus

J. S. Comaish, C. Moss, J. M. Parkin, 1991, The British journal of dermatology.

Should naevus sebaceus be excised prophylactically? A clinical audit.

M. Brundler, C. Moss, N. White, 2007, Journal of plastic, reconstructive & aesthetic surgery : JPRAS.

Congenital cutaneous lymphadenoma

R. Carr, A. Nagy, I. Colmenero, 2017, Journal of cutaneous pathology.

CHILD + ILVEN = PEN or PENCIL.

J. Burn, C. Moss, 1990, Journal of medical genetics.

Evidence for genetic homogeneity of Setleis' syndrome and focal facial dermal dysplasia

K. A. Ward, C. Moss, K. A. Ward, 1994, The British journal of dermatology.

Methotrexate treatment in 13 children with severe plaque psoriasis

B. Collin, C. Moss, A. Vani, 2009, Clinical and experimental dermatology.

Lichen planus in children: review of 26 cases

C. Moss, M. Ogboli, P. Balasubramaniam, 2008, Clinical and experimental dermatology.

Phacomatosis pigmentokeratotica and precocious puberty associated with HRAS mutation

M. Splitt, C. Moss, N. Rajan, 2017, The British journal of dermatology.

Evolving lesions of phakomatosis pigmentokeratotica1

C. Moss, S. Asad, 2004 .

Anhidrotic and achromians lesions in incontinentia pigmenti

P. Ince, C. Moss, 1987, The British journal of dermatology.

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.

E. Bauer, H. Shimizu, J. Uitto, 2014, Journal of the American Academy of Dermatology.

Seasonal occurrence of impetigo: a retrospective 8‐year review (1996–2003)

C. Moss, P. Davies, A. Loffeld, 2005, Clinical and experimental dermatology.

“NEW” SYNDROME WITH TELANGIECTASIA, DWARFISM, AND SPONDYLOEPIPHYSEAL DYSPLASIA MAY BE ROTHMUND‐THOMSON SYNDROME

C. Moss, C. Moss, 1990, Pediatric dermatology.

Human piebaldism: relationship between phenotype and site of kit gene mutation

D. Sanders, C. Moss, K. A. Ward, 1995, The British journal of dermatology.

Allogeneic bone marrow transplantation in a 7‐year‐old girl with congenital erythropoietic porphyria: a treatment dilemma

M. Badminton, C. Y. Tan, C. Moss, 2007, The British journal of dermatology.

The Birmingham Epidermolysis Bullosa Severity score: development and validation

C. Moss, A. Wong, P. Davies, 2009, The British journal of dermatology.

Lethal cardiomyopathy in epidermolysis bullosa associated with amitriptyline

P. Ramani, C. Moss, S. Taibjee, 2005, Archives of Disease in Childhood.

Supportive care in the acute phase of Stevens–Johnson syndrome and toxic epidermal necrolysis: an international, multidisciplinary Delphi‐based consensus

R. Stern, C. Bodemer, L. French, 2021, The British journal of dermatology.

Links Between Granuloma Annulare, Necrobiosis Lipoidica Diabeticorum and Childhood Diabetes: A Matter of Time?

J. Davison, C. Moss, J. Kirk, 2010, Pediatric dermatology.

Hypomelanosis of Ito/Pigmentary Mosaicism

C. Moss, S. Taibjee, 2011 .

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.

D. Kelsell, E. Sprecher, C. Mein, 2005, American journal of human genetics.

Cultured autologous keratinocyte grafting of chronic erosions in three patients with epidermolysis bullosa

J. Marsden, B. Collin, R. Papini, 2006, Clinical and experimental dermatology.

‘‘Transient’’ Bullous Disease of the Newborn may be severe

S. Baron, C. Moss, R. Eady, 2003 .

Does SNAI2 mutation cause human piebaldism and Waardenburg syndrome?

R. Spritz, C. Moss, Sara Mirhadi, 2020, American journal of medical genetics. Part A.

The Nikolsky sign in staphylococcal scalded skin syndrome

C. Moss, E. Gupta, 1998, Archives of disease in childhood.

Deletion of the SLUG (SNAI2) gene results in human piebaldism

B. Korf, R. Spritz, M. Sánchez-Martín, 2003, American journal of medical genetics. Part A.

Segmental pigmentation disorder – response

C. Moss, S. Taibjee, F. Browne, 2011, The British journal of dermatology.

Dermatology and the New Genetics

J. Savin, C. Moss, 1995 .

Genetic counselling in hypomelanosis of Ito: case report and review

J. Burn, C. Moss, C. Moss, 1988, Clinical genetics.

Duplicate reporting of patients with Rothmund-Thomson syndrome.

C. Moss, 1989, Journal of the American Academy of Dermatology.

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO).

S. Orlow, M. Golabi, J. Zonana, 2000, American journal of human genetics.

Birth incidence and outcome of harlequin ichthyosis and collodion membrane in the UK and Ireland: a national 2-year prospective surveillance study.

A. Ewer, C. Moss, Murtaza Khan, 2022, The British journal of dermatology.

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia

D. Kelsell, Y. Ishii, A. Christiano, 2006, Nature Genetics.

A current and online genodermatosis database

C. Moss, S. Leech, S. Leech, 2007, The British journal of dermatology.

The cardio‐facio‐cutaneous syndrome: a manifestation of the Noonan syndrome?

C. Moss, K. A. Ward, C. Mckeown, 1994, The British journal of dermatology.

Aplasia cutis congenita with chromosome 12q abnormality.

H. Roper, C. Moss, J. Khan, 1995, Archives of disease in childhood. Fetal and neonatal edition.

Skin lesions simulating child abuse

C. Moss, S. Srinivas, 2018 .

Minocycline for acne

R. Ferner, C. Moss, 1996, BMJ.

Comparison of cadexomer iodine and dextranomer for chronic venous ulcers

S. Shuster, C. Moss, A. Taylor, 1987, Clincal and Experimental Dermatology.

Controlled trial of Iodosorb in chronic venous ulcers

S. Shuster, C. Moss, A. Taylor, 1985 .

Kosaki overgrowth syndrome: A novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications

L. Faivre, C. Philippe, C. Thauvin-Robinet, 2020, Clinical genetics.

Targeted sequence capture and high-throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases.

Daniel S. Poon, B. Conrad, D. Kelsell, 2013, The Journal of investigative dermatology.

Congenital Livedo Reticularis and Recurrent Stroke‐like Episodes

P. Baxter, C. Moss, D. Gardner‐Medwin, 1993, Developmental medicine and child neurology.

Not non-accidental injury: a rare alternative diagnosis

C. Moss, 2009, Archives of Disease in Childhood.

Tuberculous cold abscess resembling a lymphatic malformation

C. Moss, S. Laube, D. Parikh, 2005, Clinical and experimental dermatology.

Mosaic NRAS Q61R mutation in a child with giant congenital melanocytic naevus, epidermal naevus syndrome and hypophosphataemic rickets

E. Miles, N. Shaw, I. Colmenero, 2017, Clinical and experimental dermatology.

Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12

M. Nahorski, Vykuntaraju K Gowda, C. Moss, 2018, The British journal of dermatology.

Analysis of urinary cathepsin C for diagnosing Papillon–Lefèvre syndrome

A. Vlahou, P. Fergelot, M. Battino, 2016, The FEBS journal.

Happle–Tinschert, Curry–Jones and segmental basal cell naevus syndromes, overlapping disorders caused by somatic mutations in hedgehog signalling genes: the mosaic hedgehog spectrum

S. Twigg, I. Colmenero, C. Moss, 2019, The British journal of dermatology.

Spontaneous regression of a rare tumour in a child: angiolymphoid hyperplasia with eosinophilia of the hand: case report and review of the literature.

F. Raafat, A. Satpathy, C. Moss, 2005, British journal of plastic surgery.

Genetic control of sebum excretion and acne—a twin study

C. Moss, 1989, The British journal of dermatology.

Recovery of cutaneous immune responsiveness after PUVA therapy

P. Friedmann, J. Simpson, C. Moss, 1988, The British journal of dermatology.

Organ donation from intensive care units.

G. Smith, C. Moss, G. L. Masters, 1992, BMJ.

Mid‐face toddler excoriation syndrome (MiTES): a new paediatric diagnosis

C. Owen, Vykuntaraju K Gowda, R. Hiremagalore, 2017, Clinical and experimental dermatology.

Mild ichthyosis in a 4‐year‐old boy with multiple sulphatase deficiency

S. Green, C. Moss, R. Gray, 2002, The British journal of dermatology.

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex.

J. McGrath, J. Mellerio, Lu Liu, 2017, The Journal of investigative dermatology.

Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy.

L. Biesecker, M. Topf, T. Jacques, 2018, The Journal of clinical investigation.

Diarrhea Associated with Propranolol Treatment for Hemangioma of Infancy (HOI)

H. Shahidullah, M. Parulekar, C. Moss, 2010, Pediatric dermatology.

Exclusion of an elastin gene (ELN) mutation as the cause of pseudoxanthoma elasticum (PXE) in one family

M. Hultén, A. Birley, C. Moss, 1994, Clinical genetics.

A novel ABCA12 mutation underlying a case of Harlequin ichthyosis

D. Kelsell, T. Cullup, C. Moss, 2006, The British journal of dermatology.

Ross syndrome and skin changes

N. Cartlidge, C. Moss, P. Heath, 1982, Neurology.

Degos disease: a new simulator of non‐accidental injury

H. Shahidullah, R. Malcomson, E. Wassmer, 2009, Developmental medicine and child neurology.

Thrombocytopenia in systemic lupus erythematosus responsive to dapsone.

P. Hamilton, C. Moss, 1988, BMJ.

The p.Glu477Lys Mutation in Keratin 5 Is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex.

J. McGrath, J. Mellerio, S. Hoey, 2016, The Journal of investigative dermatology.

Retrospective diagnosis of Kindler syndrome in a 37‐year‐old man

C. Moss, G. Ashton, M. A. Thomson, 2006, Clinical and experimental dermatology.

The epidemiology of epidermolysis bullosa in England and Wales: data from the national epidermolysis bullosa database *

J. McGrath, J. Mellerio, G. Petrof, 2021, The British journal of dermatology.

Antipyrine clearance in psoriasis.

M. Rawlins, S. Shuster, P. Chapman, 1981, British medical journal.

Hereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.

K. Burnand, S. Ogunbiyi, J. Deguara, 2009, Lymphology.

Disseminated clustered juvenile xanthogranuloma: an unusual morphological variant of a common condition

M. Brundler, C. Moss, M. Kaur, 2008, Clinical and experimental dermatology.

Neurocutaneous Melanosis with Leptomeningeal Melanoma

R. Grundy, S. Sgouros, C. Moss, 2001, Pediatric Neurosurgery.

Multiple cerebral abscesses in Papillon–Lefèvre syndrome

I. Chapple, H. Kanthimathinathan, A. Kay, 2013, Child's Nervous System.

Topical Therapy in Atopic Dermatitis in Children

C. Moss, D. Sathishkumar, 2016, Indian journal of dermatology.

Dilated Cardiomyopathy In Epidermolysis Bullosa: A Retrospective, Multicenter Study—Response

C. Moss, S. Taibjee, 2010, Pediatric dermatology.

Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects.

S. Banka, J. Mellerio, K. Chandler, 2022, The British journal of dermatology.

Main Plenary Session Summaries of Papers

J. Zonana, F. Keane, C. Moss, 2001 .

Cutaneous leishmaniasis in a Kosovan child treated with oral fluconazole

F. Raafat, S. Baron, C. Moss, 2004, Clinical and experimental dermatology.

Progressive nodular histiocytosis in a child with a hypothalamic tumour

C. Moss, J. Kirk, D. Sanders, 2002, British Journal of Dermatology.

Dominant dystrophic epidermolysis bullosa presenting as familial nail dystrophy

J. McGrath, J. Mellerio, A. Ilchyshyn, 2001 .

Achenbach syndrome: no need for skin biopsy

C. Moss, S. N. Cohen, 2022, Clinical and experimental dermatology.

Aplasia cutis congenita with chromosome 12 q abnormality

H. Roper, C. Moss, J. Khan, 2008 .

Subcutaneous Fat Necrosis in a Newborn Associated with Asymptomatic and Uncomplicated Hypercalcemia

C. Moss, R. Brown, M. Ogboli, 2009, Pediatric dermatology.

A congenital smooth muscle hamartoma masquerading as a reticulate vascular naevus

M. Brundler, C. Moss, J. Hughes, 2013, Clincal and Experimental Dermatology.

Topical steroid withdrawal syndrome: time to bridge the gap

C. Flohr, C. Moss, T. Burton, 2022, The British journal of dermatology.

Dermatitis artefacta in children and adolescents

C. Moss, 2015 .

Quantitation of sensitization and responsiveness to dinitrochlorobenzene in normal subjects.

S. Shuster, P. Friedmann, J. Simpson, 1983, The British journal of dermatology.

Epidermal mosaicism and Blaschko's lines.

S. Larkins, M. Stacey, P. Farndon, 1993, Journal of medical genetics.

Hereditary bullous disorders

C. Moss, 1995 .

Targeted sequence capture and high-throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases.

Daniel S. Poon, B. Conrad, D. Kelsell, 2013, The Journal of investigative dermatology.