THE HYPERTELORISM MICROTIA CLEFTING SYNDROMEBARAITSER M.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 387-388; BIBL. 2 REF.Article

QUESTION AND ANSWERBARAITSER M.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 4; PP. 300; BIBL. 2 REF.Article

GENETICS OF MOEBIUS SYNDROME.BARAITSER M.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 6; PP. 415-417; BIBL. 13 REF.Article

RELEVANCE OF A FAMILY HISTORY OF SEIZURESBARAITSER M.1983; ARCHIVES OF DISEASES IN CHILDHOOD; ISSN 0003-9888; GBR; DA. 1983; VOL. 58; NO 6; PP. 404-405; BIBL. 5 REF.Article

The orofaciodigital (OFD) syndromesBARAITSER, M.Journal of medical genetics. 1986, Vol 23, Num 2, pp 116-119, issn 0022-2593Article

THE JOHANSON-BLIZZARD SYNDROMEBARAITSER M; HODGSON SV.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 302-303; BIBL. 8 REF.Article

RECESSIVELY INHERITED BRACHYDACTYLY TYPE CBARAITSER M; BURN J.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 128-129; BIBL. 2 REF.Article

GENETIC STUDY OF NARCOLEPTIC SYNDROMEBARAITSER M; PARKES JD.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 4; PP. 254-259; BIBL. 14 REF.Article

THE RUBINSTEIN-TAYLOR SYNDROME: OCCURRENCE IN TWO SETS OF IDENTICAL TWINSBARAITSER M; PREECE MA.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 4; PP. 318-320; BIBL. 10 REF.Article

MICROCEPHALY AND INTRACRANIAL CALCIFICATION IN TWO BROTHERSBARAITSER M; BRETT EM; PIESOWICZ AT et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 210-212; BIBL. 11 REF.Article

PERIPHERAL AND CENTRAL SOMATOSENSORY NERVE CONDUCTION DEFECTS IN FRIEDREICH'S ATAXIAJONES SJ; BARAITSER M; HALLIDAY AM et al.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1980; VOL. 43; NO 6; PP. 495-503; BIBL. 30 REF.Article

A RECESSIVELY INHERITED WINDMILL-VANE CAMPTODACTYLY/ICHTHYOSIS SYNDROMEBARAITSER M; BURN J; FIXSEN J et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 2; PP. 125-127; BIBL. 5 REF.Article

LENZ MICROPHTHALMIA - A CASE REPORTBARAITSER M; WINTER RM; TAYLOR DSI et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 2; PP. 99-101; BIBL. 5 REF.Article

A FEMALE INFANT WITH FEATURES OF MOHR AND MAJEWSKI SYNDROMES: VARIABLE EXPRESSION, A GENETIC COMPOUND, OR A DISTINCT ENTITY.BARAITSER M; BURN J; FIXEN J et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 1; PP. 65-67; BIBL. 5 REF.Article

A NEW CRANIOSYNOSTOSIS/MENTAL RETARDATION SYNDROME DIAGNOSED BY FETOSCOPYBARAITSER M; RODECK C; GARNER A et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 1; PP. 12-15; BIBL. 3 REF.Article

AUTOSOMAL DOMINANT ASYMMETRICAL RADIAL DYSPLASIA, DYSMORPHIC FACIES, AND CONDUCTIVE HEARING LOSS (FACIOAURICULO=RADIAL DYSPLASIA)HARDING AE; HALL CM; BARAITSER M et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 110-115; BIBL. 18 REF.Article

A NEW ALOPECIA/MENTAL RETARDATION SYNDROMEBARAITSER M; CARTER CO; BRETT EM et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 1; PP. 64-65; BIBL. 3 REF.Article

Johanson-Blizzard syndromeHURST, J. A; BARAITSER, M.Journal of medical genetics. 1989, Vol 26, Num 1, pp 45-48, issn 0022-2593Article

A Noonan-like short stature syndrome with sparse hairBARAITSER, M; PATTON, M. A.Journal of medical genetics. 1986, Vol 23, Num 2, pp 161-164, issn 0022-2593Article

Neural tube defects as an X-linked conditionBARAITSER, M; BURN, J.American journal of medical genetics. 1984, Vol 17, Num 1, pp 383-385, issn 0148-7299Article

PITFALLS OF GENETIC COUNSELLING IN PFEIFFER'S SYNDROMEBARAITSER M; BOWEN BRAVERY M; SALDANA GARCIA P et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 250-256; BIBL. 8 REF.Article

Coffin-siris syndromeLEVY, P; BARAITSER, M.Journal of medical genetics. 1991, Vol 28, Num 5, pp 338-341, issn 0022-2593Article

Hereditary neurocutaneous angiomatous malformations: autosomal dominant inheritance in two familiesHURST, J; BARAITSER, M.Clinical genetics. 1988, Vol 33, Num 1, pp 44-48, issn 0009-9163Article

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